CFR section
21 CFR 820.60: Identification
PART 820-QUALITY SYSTEM REGULATION · Subpart F-Identification and Traceability
Key facts
| Citation | 21 CFR 820.60 |
|---|---|
| Section | Identification |
| Part | PART 820-QUALITY SYSTEM REGULATION |
| Subpart | Subpart F-Identification and Traceability |
| Subchapter | 21 CFR H Medical Devices |
| Product types cited | Devices, Drugs |
| Regulation text (excerpt) | Each manufacturer shall establish and maintain procedures for identifying product during all stages of receipt, production, distribution, and installation to prevent mixups. |
At a glance
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About CFR sections cited by the FDA
Title 21 of the Code of Federal Regulations contains the FDA's regulations, including current good manufacturing practice and quality system requirements that inspections cite.