CFR section
21 CFR 803.32: If I am a user facility, what information must I submit in my individual adverse event reports?
PART 803-MEDICAL DEVICE REPORTING · Subpart C-User Facility Reporting Requirements
Key facts
| Citation | 21 CFR 803.32 |
|---|---|
| Section | If I am a user facility, what information must I submit in my individual adverse event reports? |
| Part | PART 803-MEDICAL DEVICE REPORTING |
| Subpart | Subpart C-User Facility Reporting Requirements |
| Subchapter | 21 CFR H Medical Devices |
| Product types cited | Devices |
At a glance
- 1–9 Inspections citing this section
- None 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.