subchapter_subject: "ANIMAL DRUGS, FEEDS, AND RELATED PRODUCTS"
part_code: "507"
part_subject: "CURRENT GOOD MANUFACTURING PRACTICE, HAZARD ANALYSIS, AND RISK-BASED PREVENTIVE CONTROLS FOR FOOD FOR ANIMALS"
subpart_code: "F"
subpart_subject: "Requirements Applying to Records That Must Be Established and Maintained"
section_number: "507.200"
section_subject: "Records subject to the requirements of this subpart."
cfr_reference: "21 CFR 507.200"
title_name: "Title 21"
title_subject: "Food and Drugs"
parts_covered: "Parts 500 to 599"
revised_date: "Revised as of April 1, 2019"
publication_date: "As of April 1, 2019"
contains_description: "Containing a codification of documents of general applicability and future effect"
publication_info: "Published by the Office of the Federal Register National Archives and Records Administration as a Special Edition of the Federal Register"
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(a)Except as provided by paragraphs (d) and (e) of this section, all records required by this part are subject to all requirements of this subpart.
(b)Records obtained by FDA in accordance with this part are subject to the disclosure requirements under part 20 of this chapter.
(c)All records required by this part must be made promptly available to a duly authorized representative of the Secretary of Health and Human Services for official review and copying upon oral or written request.
(d)The requirements of § 507.206 apply only to the written food safety plan.
(e)The requirements of § 507.202(a)(2), (4), and (5) and (b) do not apply to the records required by § 507.7.