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e-CFR data is current as of July 31, 2020

Title 21Chapter ISubchapter HPart 806Subpart B → §806.30


Title 21: Food and Drugs
PART 806—MEDICAL DEVICES; REPORTS OF CORRECTIONS AND REMOVALS
Subpart B—Reports and Records


§806.30   FDA access to 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.

[63 FR 42233, Aug. 7, 1998]

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