CFR section
21 CFR 820.100(a)(6): Corrective and preventive action
PART 820-QUALITY SYSTEM REGULATION · Subpart J-Corrective and Preventive Action
Key facts
| Citation | 21 CFR 820.100(a)(6) |
|---|---|
| Section | Corrective and preventive action |
| Part | PART 820-QUALITY SYSTEM REGULATION |
| Subpart | Subpart J-Corrective and Preventive Action |
| Subchapter | 21 CFR H Medical Devices |
| Product types cited | Biologics, Devices, Drugs |
| Regulation text (excerpt) | (6) Ensuring that information related to quality problems or nonconforming product is disseminated to those directly responsible for assuring the quality of such product or the prevention of such problems; and |
At a glance
- 10–99 Inspections citing this section
- 1–9 Warning letters citing this section
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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.