GroundRules
21 CFR 806.30: FDA access to records.
Where this section sits in the code
- Title 21—Food and Drugs
- CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES
- SUBCHAPTER H—MEDICAL DEVICES
- PART 806—MEDICAL DEVICES; REPORTS OF CORRECTIONS AND REMOVALS
- Subpart B—Reports and Records
Each device manufacturer or importer required under this part to maintain records and every person who is in charge or custody of such records shall, upon request of an officer or employee designated by FDA and under section 704(e) of the act, permit such officer or employee at all reasonable times to have access to, and to copy and verify, such records and reports.
Collected 2026-08-27T02:24:47Z. Source file · JSON