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Regulations last checked for updates: May 14, 2025
Title 21 - Food and Drugs last revised: May 12, 2025
All Titles
Title 21
Chapter I
Part 1002 - PART 1002—RECORDS AND REPORTS
Subpart A [§ 1002.1 - § 1002.7] - Subpart A—General Provisions
Subpart B [§ 1002.10 - § 1002.13] - Subpart B—Required Manufacturers' Reports for Listed Electronic Products
Subpart C [§ 1002.20 - § 1002.20] - Subpart C—Manufacturers' Reports on Accidental Radiation Occurrences
Subpart D [§ 1002.30 - § 1002.31] - Subpart D—Manufacturers' Records
Subpart E [§ 1002.40 - § 1002.42] - Subpart E—Dealer and Distributor Records
Subpart F [§ 1002.50 - § 1002.51] - Subpart F—Exemptions From Records and Reports Requirements
authority:
21 U.S.C. 352
,
360
,
360
i,
360
j,
360
hh-360ss,
371
,
374
source:
38 FR 28625, Oct. 15, 1973, unless otherwise noted.
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