CFR section
21 CFR 820.40: Document controls
PART 820-QUALITY SYSTEM REGULATION · Subpart D-Document Controls
Key facts
| Citation | 21 CFR 820.40 |
|---|---|
| Section | Document controls |
| Part | PART 820-QUALITY SYSTEM REGULATION |
| Subpart | Subpart D-Document Controls |
| Subchapter | 21 CFR H Medical Devices |
| Product types cited | Biologics, Devices, Drugs, Food/Cosmetics, General, Other_Regulations |
At a glance
- 1,000+ Inspections citing this section
- 100–999 Warning letters citing this section
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
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.