21 CFR Part 1002
PART 1002—RECORDS AND REPORTS
- PART 1002—RECORDS AND REPORTS
- Chapter I—Food and Drug Administration, Department of Health and Human Services › Subchapter J—Radiological Health
- Subpart A—General Provisions
- § 1002.1 Applicability.
- § 1002.2 [Reserved]
- § 1002.3 Notification to user of performance and technical data.
- § 1002.4 Confidentiality of information.
- § 1002.7 Submission of data and reports.
- Subpart B—Required Manufacturers' Reports for Listed Electronic Products
- § 1002.10 Product reports.
- § 1002.11 Supplemental reports.
- § 1002.12 Abbreviated reports.
- § 1002.13 Annual reports.
- Subpart C—Manufacturers' Reports on Accidental Radiation Occurrences
- § 1002.20 Reporting of accidental radiation occurrences.
- Subpart D—Manufacturers' Records
- § 1002.30 Records to be maintained by manufacturers.
- § 1002.31 Preservation and inspection of records.
- Subpart E—Dealer and Distributor Records
- § 1002.40 Records to be obtained by dealers and distributors.
- § 1002.41 Disposition of records obtained by dealers and distributors.
- § 1002.42 Confidentiality of records furnished by dealers and distributors.
- Subpart F—Exemptions From Records and Reports Requirements
- § 1002.50 Special exemptions.
- § 1002.51 Exemptions for manufacturers of products intended for the U.S. Government.
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