U.S. Supreme Court, (June 09, 1980)
Docket number: 79-521
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U.S. Code - Title 15: Commerce and Trade - 15 USC 2074 - Sec. 2074. Private remedies
U.S. Code - Title 15: Commerce and Trade - 15 USC 2057 - Sec. 2057. Banned hazardous products
U.S. Code - Title 15: Commerce and Trade - 15 USC 2055 - Sec. 2055. Public disclosure of information
U.S. Supreme Court - Burlington Northern R. Co. v. Oklahoma Tax Comm'n, 481 U.S. 454 (1987)
U.S. Supreme Court CONSUMER PRODUCT SAFETY COMM'N v. GTE SYLVANIA, 447 U.S. 102 (1980) 447 U.S. 102
CONSUMER PRODUCT SAFETY COMMISSION ET AL. v. GTE SYLVANIA, INC., ET AL. CERTIORARI TO THE UNITED STATES COURT OF APPEALS FOR THE THIRD CIRCUIT. No. 79-521. Argued April 14, 1980. Decided June 9, 1980. Section 6 (b) (1) of the Consumer Product Safety Act (CPSA) requires that, at least 30 days prior to the "public disclosure of any information" pertaining to a consumer product obtained by the Consumer Product Safety Commission (Commission) pursuant to its information-gathering authority, the Commission must notify the manufacturer and provide it with a summary of the information to be disclosed, if the product is to be designated or described in such a way as to permit the public to ascertain readily the manufacturer's identity; that the manufacturer be given a reasonable opportunity to submit comments regarding the information; and that the Commission "take reasonable steps to assure" that such information is "accurate" and that disclosure is "fair in the circumstances and reasonably related to effectuating the purposes" of the CPSA. In the instant case, the Commission, upon receiving Freedom of Information Act (FOIA) requests and without complying with 6 (b) (1), decided to release certain accident reports that it had obtained from respondent manufacturers and that were accompanied, for the most part, by claims of confidentiality. The District Court permanently enjoined the Commission from disclosing the materials, rejecting its contention that 6 (b) (1) applies only when the Commission affirmatively undertakes to disclose information to the public but not when it merely complies with a request for information under the FOIA. The Court of Appeals affirmed. Held: Section 6 (b) (1) governs the disclosure of records by the Commission pursuant to a request under the FOIA. Pp. 108-124. (a) Nothing in 6 (b) (1)'s language, or in any other provision of the CPSA, supports the claim that 6 (b) (1) is limited to disclosures initiated by the Commission, a disclosure pursuant to the FOIA being accurately characterized as a "public disclosure" within the plain meaning of 6 (b) (1). Moreover, 6 (b) (2), which contains specific exceptions to 6 (b) (1)'s requirements, does not include the disclosure of information in response to an FOIA request. And 25 (c) of the CPSA - designating certain reports as "public information" notwithstanding that they might be exempted from disclosure under the [Page 447 U.S. 102, 103] FOIA and thus within the scope of 6 (a) (1), which incorporates by reference the exemptions of the FOIA - specifically makes the disclosure of the information subject to the limitations of 6 (b) whether it be "affirmatively" released by the Commission or released pursuant to an FOIA request. Pp. 108-110. (b) Neither the legislative history of the CPSA prior to its enactment nor subsequent legislative and administrative interpretations of 6 (b) (1) warrant construing 6 (b) (1) as being limited to the Commission's "affirmative" disclosures. Pp. 110-120. (c) Applicability of 6 (b) (1) to FOIA requests is not precluded on the alleged ground that the Commission would be unable to comply with FOIA time requirements for handling disclosure requests and administrative appeals from refusals to disclose. Such an argument assumes that the Commission must comply with FOIA time limitations, but its Exemption 3 states that the FOIA does not apply to matters that are specifically exempted from disclosure by another statute which requires that the matters be withheld from the public in such a manner as to leave no discretion on the issue, or which establishes particular criteria for withholding or refers to particular types of matters to be withheld. Here, 6 (b) (1) sets forth sufficiently definite standards to fall within the scope of Exemption 3. Pp. 121-123. (d) The argument that requiring the Commission to comply with 6 (b) (1) in meeting FOIA requests will impose insurmountable burdens on the agency is entirely speculative. Moreover, any increased burdens imposed on the Commission were intended by Congress in striking an appropriate balance between the interests of consumers and the need for fairness and accuracy with respect to information disclosed by the Commission and thus the claim of undue burdens is properly addressed to Congress, not this Court. Pp. 123-124. 598 F.2d 790, affirmed. REHNQUIST, J., delivered the opinion for a unanimous Court. Peter Buscemi argued the cause pro hac vice for petitioners. With him on the briefs were Solicitor General McCree, Assistant Attorney General Daniel, Deputy Solicitor General Geller, Leonard Schaitman, Mark N. Mutterperl, and Andrew S. Krulwich. Bernard G. Segal argued the cause for respondents. With him on the brief were Charles C. Hileman III, Ira P. Tiger, [Page 447 U.S. 102, 104] Deena Jo Schneider, Robert W. Steele, Alan M. Grimaldi, Harry L. Shniderman, H. James Conaway, Jr., Januar D. Bove, Jr., Stephen B. Clarkson, Charles S. Crompton, Jr., Ira M. Millstein, Peter Gartland, David Fleischer, Burton Y. Weitzenfeld, Michael A. Stiegel, William F. Patten, and H. Woodruff Turner.* [Footnote *] Richard A. Lowe filed a brief for the Consumer Federation of America as amicus curiae urging reversal. MR. JUSTICE REHNQUIST delivered the opinion of the Court. The question presented is whether 6 (b) (1) of the Consumer Product Safety Act, 15 U.S.C. 2055 (b) (1), governs the disclosure of records by the Consumer Product Safety Commission pursuant to a request under the Freedom of Information Act. We granted certiorari to review a judgment of the Court of Appeals for the Third Circuit because of the importance of the question and because of a conflict in the Circuits.[Footnote 1] 444 U.S. 979. I In 1972, Congress enacted the Consumer Product Safety Act (CPSA), 86 Stat. 1207, 15 U.S.C. 2051 et seq., in order, inter alia, "to protect the public against unreasonable risks of injury associated with consumer products" and "to assist consumers in evaluating the comparative safety of consumer products." 15 U.S.C. 2051 (b) (1) and (2). The CPSA created the Consumer Product Safety Commission (Commission) to carry out the statutory purposes. 15 U.S.C. 2053. The Commission's powers include the authority to collect and disseminate product safety information, 15 U.S.C. 2054 (a) (1), to conduct research and tests on consumer products, 15 U.S.C. 2054 (b) (1) and (2), to promulgate safety standards, 15 U.S.C. 2056, and to ban hazardous products, 15 U.S.C. 2057. [Page 447 U.S. 102, 105] Section 6 of the CPSA, 86 Stat. 1212, 15 U.S.C. 2055, regulates the "public disclosure" of information by the Commission. Section 6 (b) (1), with which we deal here, requires the Commission, at least 30 days before the public disclosure of information pertaining to a consumer product, to notify the manufacturer and to provide it with a summary of the information to be disclosed, if the product is to be designated or described in such a way as to permit the public to ascertain readily the manufacturer's identity. The manufacturer must be given a reasonable opportunity to submit comments regarding the information. And the Commission must take reasonable steps to assure that such information is accurate and that disclosure is "fair in the circumstances and reasonably related to effectuating the purposes" of the CPSA. If the Commission subsequently finds that it has made public disclosure of inaccurate or misleading information that adversely reflects on a manufacturer's products or practices, the Commission must "publish a retraction" in a manner "similar to that in which such disclosure was made. . . ."[Footnote 2] [Page 447 U.S. 102, 106] The relevant facts are set forth in a case decided by this Court earlier this Term, GTE Sylvania, Inc. v. Consumers Union, 445 U.S. 375 (1980), and need not be restated in detail. Briefly, the Commission obtained from respondents various accident reports, most of which were accompanied by claims of confidentiality. The Commission subsequently decided, after receiving Freedom of Information Act (FOIA) requests from the Consumers Union of the United States, Inc., and the Public Citizen's Health Research Group (the requesters), to release even those accident reports that were claimed to be confidential. Not surprisingly, lawsuits were soon filed in several Federal District Courts. See GTE Sylvania, Inc. v. Consumers Union, supra, at 378, n. 1. [Page 447 U.S. 102, 107] The District Court for the District of Delaware ultimately granted respondents' motion for summary judgment and permanently enjoined the Commission from disclosing the submitted accident reports, as well as data compiled on a computer printout from those reports. 443 F. Supp. 1152 (1977).[Footnote 3] The District Court rejected the Commission's contention that 6 (b) (1) applies only when the Commission affirmatively undertakes to disclose information to the public, but not when it merely complies with a request for information under the FOIA. It held that 6 (b) (1) is applicable to disclosures in response to FOIA requests and that it establishes particular criteria for withholding information, thereby falling within the scope of Exemption 3 of the FOIA, 5 U.S.C. 552 (b) (3). It also found that the Commission failed to comply with 6 (b) (1) procedures in this case. Thus, it concluded that the release of the accident reports would be contrary to the CPSA. 443 F. Supp., at 1162. The Court of Appeals for the Third Circuit affirmed. 598 F.2d 790 (1979). After thoroughly examining the language and legislative history of 6 (b) (1), it concluded that "Congress did not intend that provision to apply only to Commission press releases, news conferences, publication of reports and other forms of `affirmative disclosure' of information obtained under the Act." 598 F.2d, at 811. Rather, "the information disclosure requirements of the CPSA were meant to protect manufacturers from the harmful effects of inaccurate or misleading public disclosure by the Commission, through any means, of material obtained pursuant to its broad information-gathering powers. The policies designed to be served by section 6 (b) (1) would be severely undermined, if not eviscerated, were the Commission's interpretation to prevail." Id., at 811-812. [Page 447 U.S. 102, 108] Petitioners repeat their contention here that 6 (b) (1) was intended to provide safeguards for the release of information by the Commission only when the Commission makes public disclosures of information on its own initiative in carrying out its responsibilities under the CPSA. When information is released in this fashion, they argue, the Commission explicitly or implicitly represents that it believes the disclosed information to be true and that the public should rely on it. Brief for Petitioners 10. When the Commission merely releases information in response to an FOIA request, by contrast, they claim the Commission is obliged to release whatever materials it possesses and need not comply with 6 (b) (1), because it has not made any express or implied statement regarding the documents released or the extent to which those documents reflect agency policy. Brief for Petitioners 11. Although there is some support for petitioners' interpretation of 6 (b) (1) in legislative history contained in a Conference Report four years after the enactment of that section, see Part IV, infra, we agree with the Court of Appeals' determination that "legislative history" of this sort cannot be viewed as controlling. II We begin with the familiar canon of statutory construction that the starting point for interpreting a statute is the language of the statute itself. Absent a clearly expressed legislative intention to the contrary, that language must ordinarily be regarded as conclusive. Section 6 (b) (1) by its terms applies to the "public disclosure of any information" obtained by the Commission pursuant to its authority under the CPSA, and to any information "to be disclosed to the public in connection therewith." (Emphasis added.) Nothing in the language of that section, or in any other provision of the CPSA, supports petitioners' claim that 6 (b) (1) is limited to disclosures initiated by the Commission. And as a matter of common usage the term [Page 447 U.S. 102, 109] "public" is properly understood as including persons who are FOIA requesters. A disclosure pursuant to the FOIA would thus seem to be most accurately characterized as a "public disclosure" within the plain meaning of 6 (b) (1).[Footnote 4] Section 6 (b) (2) of the CPSA, 15 U.S.C. 2055 (b) (2), contains specific exceptions to the requirements of 6 (b) (1).[Footnote 5] But the list of exceptions does not include the disclosure of information in response to an FOIA request. If Congress had intended to exclude FOIA disclosures from 6 (b) (1) it could easily have done so explicitly in this section as it did with respect to the other listed exceptions. That Congress was aware of the relationship between 6 and the FOIA when it enacted the CPSA is exhibited by the fact that Congress in 6 (a) (1) specifically incorporated by reference the nine exemptions of the FOIA, 5 U.S.C. 552 (b). We are consequently reluctant to conclude that Congress' failure to include FOIA requests within the exceptions to 6 (b) (1) listed in 6 (b) (2) was unintentional. Finally, 25 (c) of the CPSA, 15 U.S.C. 2074 (c), further supports the conclusion that 6 (b) (1) was not intended to distinguish between information disclosed to the public [Page 447 U.S. 102, 110] pursuant to FOIA requests and information disclosed at the initiative of the Commission.[Footnote 6] Section 25 (c) designates accident and investigation reports that do not identify injured parties and their physicians, and reports on research and demonstration projects as "public information" notwithstanding the fact that they might be exempted from disclosure under the FOIA and thus within the scope of 6 (a) (1). Section 25 (c), however, specifically makes the disclosure of this information subject to the limitations of 6 (a) (2) and 6 (b), whether it be "affirmatively" released by the Commission or released pursuant to an FOIA request. The language of the CPSA thus provides little basis for accepting petitioners' claim that 6 (b) (1) does not apply to information released by the Commission in response to FOIA requests. III Petitioners next argue that the legislative history of the CPSA requires the conclusion that 6 (b) (1) is inapplicable to FOIA requests despite the language of the statute. In making their argument, petitioners concede that "the pre-enactment history of this legislation does not directly address the precise issue of statutory construction involved in this case." Brief for Petitioners 33. They nonetheless maintain that the principal concern underlying the adoption of the section was the danger that the Commission might on its own initiative disseminate findings, reports, and other product information harmful to manufacturers without first assuring [Page 447 U.S. 102, 111] the fairness and accuracy of the disclosure. We agree with petitioners that industry representatives were concerned about the harms resulting from information affirmatively disclosed by an agency. But petitioners have failed to establish that industry concerns were limited to information disclosed in this fashion.[Footnote 7] More importantly, a full examination of the legislative history of the CPSA prior to its enactment indicates that for purposes of 6 (b) (1) no distinction was made between information affirmatively disclosed by the Commission and information released pursuant to the FOIA. The CPSA gave the Commission broad powers to gather, analyze, and disseminate vast amounts of private information. In granting the Commission such authority, Congress adopted safeguards specifically designed to protect manufacturers' reputations from damage arising from improper disclosure of [Page 447 U.S. 102, 112] information gathered and received by the Commission. The House Report on the CPSA states: "If the Commission is to act responsibly and with adequate basis, it must have complete and full access to information relevant to its statutory responsibilities. Accordingly, the committee has built into this bill broad information-gathering powers. It recognizes that in so doing it has recommended giving the Commission the means of gaining access to a great deal of information which would not otherwise be available to the public or to Government. Much of this relates to trade secrets or other sensitive cost and competitive information. Accordingly, the committee has written into section 6 of the bill detailed requirements and limitations relating to the Commission's authority to disclose information which it acquires in the conduct of its responsibilities under this act." H. R. Rep. No. 92-1153, p. 31 (1972).[Footnote 8] [Page 447 U.S. 102, 113] The House Report does not provide any indication that the safeguards for the release of CPSA information are inapplicable when the Commission discloses information in response to an FOIA request. And in its explanatory comments on 6 (b) (1) the Report makes no distinction whatsoever between information released at the initiative of the Commission [Page 447 U.S. 102, 114] and information disclosed pursuant to an FOIA request. Rather, it states: "Before disseminating any information which identifies the manufacturer or private labeler of a product, the Commission is directed to give the manufacturer or private labeler 30 days in which to comment on the proposed disclosure of information. This procedure is intended to permit the manufacturer or private labeler an opportunity to come forward with explanatory data or other relevant information for the Commission's consideration." H. R. Rep. No. 92-1153, supra, at 32 (emphasis added). Nor does the Conference Report contain any suggestion that 6 (b) (1) does not apply to FOIA requests. As observed by the Court of Appeals, the "conferees' description of section 6 (b) (1) is instructive in that the accuracy and fairness requirements for `publicly disclosed information' are mentioned in almost the same breath as the description of section 6 (a) (1), stating that no information need be `publicly disclosed' by the Commission if it is exempt from disclosure under the FOIA." 598 F.2d, at 809.[Footnote 9] Further support for this construction of 6 (b) (1) can be found in examining comments made with respect to earlier versions of the House bill.[Footnote 10] In commenting on the disclosure [Page 447 U.S. 102, 115] provisions of the administration bill, H. R. 8110, Representative Moss, chairman of the Subcommittee on Commerce and Finance, which was considering the House bills, stated: "I am sure the subcommittee will want to examine carefully this proposed change in the Freedom of Information Act." Sub-committee Hearings, pt. 2, p. 300.[Footnote 11] The operative information-disclosure requirements contained in 4 (c) of H. R. 8110, absent a requirement that the Commission publish manufacturers' comments, were nonetheless enacted into law in 6 (b). See n. 8, supra. Section 4 (c) and the provision that was finally enacted as 6 (b) by their terms include both affirmative disclosures by the Commission and information released pursuant to the FOIA. And the Department of Health, Education, and Welfare, the agency that drafted H. R. 8110, stated in its section-by-section analysis of the bill: "Section 4 (c) would protect the Secretary's refusal to disclose information not required to be released by the [FOIA], and would expressly prohibit his disclosure of commercial secrets, or of illness or injury data revealing [the] identity of the victim. "It would also require the provision of thirty days notice to the manufacturer of any consumer product prior to the Secretary's public disclosure of information respecting that product, if such information would reveal the manufacturer's identity." Subcommittee Hearings, pt. 1, p. 188. [Page 447 U.S. 102, 116] These comments clearly do not support petitioners' reading of the present disclosure requirements of the CPSA. And the General Counsel of the Department of Commerce, in opposing the Senate's less restrictive proposal for the disclosure of information by the Commission, wrote: "[W]e believe that in the interest of fairness the disclosure of any information should be attendant with safeguards. These include prior notice to manufacturers, the right of the manufacturer to rebut false information, and a requirement that the information be fair and accurate." S. Rep. No. 92-749, p. 100 (1972) (emphasis added). The legislative history of 6 (b) (1) thus fails to establish that petitioners' proposed distinction should be read into the section. IV Petitioners also contend that legislative interpretations of 6 (b) (1) made after the section was enacted and the Commission's administrative interpretation of that section support their proposed construction. Petitioners first rely on a statement by Representative Moss, one of the sponsors of the House bill. In testimony before a congressional Oversight Subcommittee, then Commission Chairman Richard O. Simpson explained that the Commission interpreted 6 (b) (1) to be inapplicable to FOIA requests. Representative Moss then remarked: "As the primary author of both acts, I am inclined to agree with you." Regulatory Reform: Hearings before the Subcommittee on Oversight and Investigations of the House Committee on Interstate and Foreign Commerce, 94th Cong., 2d Sess., Vol. IV, pp. 7-8 (1976). Petitioners also note that when Congress added 29 (e), 15 U.S.C. 2078 (e), to the CPSA in the Consumer Product Safety Commission Improvements Act of 1976, the Conference Committee explained the joint operation of the new section and 6 (b) as follows:"The requirement that the Commission comply with section 6 (b) prior to another Federal agency's public [Page 447 U.S. 102, 117] disclosure of information obtained under the Act is not intended by the conferees to supersede or conflict with the requirements of the Freedom of Information Act (5 U.S.C. 552 (a) (3) and (a) (6)). The former relates to public disclosure initiated by the Federal agency while the latter relates to disclosure initiated by a specific request from a member of the public under the Freedom of Information Act." H. R. Conf. Rep. No. 94-1022, p. 27 (1976) (emphasis added).[Footnote 12] In evaluating the weight to be attached to these statements, we begin with the oft-repeated warning that "the views of a subsequent Congress form a hazardous basis for inferring the intent of an earlier one." United States v. Price, 361 U.S. 304, [Page 447 U.S. 102, 118] 313 (1960), quoted in United States v. Philadelphia National Bank, 374 U.S. 321, 348-349 (1963).[Footnote 13] And ordinarily even the contemporaneous remarks of a single legislator who sponsors a bill are not controlling in analyzing legislative history. Chrysler Corp. v. Brown, 441 U.S. 281, 311 (1979). We do not think that either Representative Moss' isolated remark or the post hoc statement of the Conference Committee with respect to 6 (b) is entitled to much weight here. While Representative Moss claimed sponsorship of the CPSA generally, he was not a sponsor of the original bill that ultimately provided that legislation with its provisions governing information disclosure. Rather he authored another bill, H. R. 8157, that contained much less restrictive disclosure requirements than those ultimately adopted.[Footnote 14] His statement [Page 447 U.S. 102, 119] is thus not one that provides a reliable indication as to congressional intention.[Footnote 15] An examination of the statement of the Conference Committee, as the Court of Appeals concluded, reveals that it also is not persuasive authority in support of petitioners' position. Section 29 (e) by its terms does not purport to interpret the scope of 6 (b). Rather, it deals solely with the release of accident and investigation reports by the Commission to other agencies. See n. 12, supra. And as the Court of Appeals stated: "[T]he conference committee statement was made in the context of approving legislation that contained numerous and extensive amendments to the Consumer Product Safety Act; yet the problem before us here was not otherwise addressed by Congress in enacting the Improvements Act. The interpretation of section 6 (b) espoused by the conferees was not mentioned by the House committee that drafted the Improvements Act. See H. R. Rep. No. 94-325, 94th Cong., 1st Sess. 18 (1975). The Senate version of the Improvements Act did not contain a provision amending section 29. [H. R. Conf. Rep. No. 94-1022, p. 26.] In the debates in the House the amendment to section 29, and the relationship between section 6 (b) and the FOIA, were not [Page 447 U.S. 102, 120] mentioned. Nor was the conferees' interpretation of section 6 (b) mentioned in either House when the conference report was debated. See 122 Cong. Rec. 10,811 (House approval of the conference report); id., 11,585 (Senate approval) (1976)." 598 F.2d, at 810-811. In light of this background, the statement of the Conference Committee is far from authoritative as an expression of congressional will under the oft-quoted factors enunciated in Skidmore v. Swift & Co., 323 U.S. 134, 140 (1944).[Footnote 16] For the same reasons, we reject petitioners' contention that the Commission's 1977 administrative interpretation should be afforded the degree of deference necessary for it to prevail here. See 42 Fed. Reg. 54304 et seq. (1977). This case presents a narrow legal issue that is readily susceptible of judicial resolution. Nor are we presented here with a situation in which there has been a longstanding contemporaneous administrative construction upon which those subject to the jurisdiction of the agency would have been likely to rely.[Footnote 17] [Page 447 U.S. 102, 121] V Petitioners next argue that the interpretation of 6 (b) (1) by the Court of Appeals is inconsistent with the FOIA time requirements for the release of information. The FOIA requires an agency to "determine within ten days . . . whether to comply with [an FOIA] request" and to notify the requester "immediately" of the agency's determination. 5 U.S.C. 552 (a) (6) (A) (i). The FOIA also requires an agency to resolve any administrative appeal of a refusal to disclose within 20 days after the filing of the appeal. 552 (a) (6) (A) (ii). Petitioners claim that if 6 (b) (1) applies to FOIA requests the Commission will be unable to comply with FOIA time requirements. Petitioners' argument assumes that despite the specific procedural safeguards set forth in 6 (b) (1) the Commission must comply with FOIA time limitations. Federal agencies, however, are granted discretion to refuse FOIA requests when the requested material falls within one of the nine statutory exemptions set forth in 5 U.S.C. 552 (b). Exemption 3 of the FOIA, 5 U.S.C. 552 (b) (3), states that the FOIA does not apply to matters that are "specifically exempted from disclosure by statute (other than section 552b of this title), provided that such statute (A) requires that the matters be withheld from the public in such a manner as to leave no discretion on the issue, or (B) establishes particular criteria for withholding or refers to particular types of matters to be withheld."[Footnote 18] [Page 447 U.S. 102, 122] Here 6 (b) (1) sets forth sufficiently definite standards to fall within the scope of Exemption 3. It does not grant the Commission broad discretion to refuse to comply with FOIA requests. Rather, it requires that the Commission "take reasonable steps to assure" (1) that the information is "accurate," (2) that disclosure will be "fair in the circumstances," and (3) that disclosure will be "reasonably related to effectuating the purposes of [the CPSA]."[Footnote 19] We therefore do not [Page 447 U.S. 102, 123] believe there is any insoluble conflict between 6 (b) (1) and the FOIA.[Footnote 20] VI Finally, petitioners argue that requiring the Commission to comply with 6 (b) (1) in meeting FOIA requests will impose insurmountable burdens on the agency. In making this claim, petitioners state that the Commission receives nearly 8,000 FOIA requests annually. The extent to which these requests will present problems of fairness and accuracy with respect to the information released by the Commission is entirely speculative. And in light of the fact that Exemption 3 is applicable to the disclosure of information controlled by 6 (b) (1), we do not think these burdens will prove to be unbearable. Most importantly, our interpretation of the language and legislative history of 6 (b) (1) reveals that any increased burdens imposed on the Commission as a result of its compliance with 6 (b) (1) were intended by Congress in striking an appropriate balance between the interests of [Page 447 U.S. 102, 124] consumers and the need for fairness and accuracy with respect to information disclosed by the Commission. Thus, petitioners' claim that the Commission's compliance with the requirements of 6 (b) (1) will impose undue burdens on the Commission is properly addressed to Congress, not to this Court. For the foregoing reasons, the judgment of the Court of Appeals for the Third Circuit is Affirmed. FootnotesFootnote 1 The decision below, 598 F.2d 790 (1979), is in direct conflict with Pierce & Stevens Chemical Corp. v. 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