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e-CFR data is current as of March 4, 2021

Title 21Chapter ISubchapter HPart 822Subpart G → §822.36


Title 21: Food and Drugs
PART 822—POSTMARKET SURVEILLANCE
Subpart G—Records and Reports


§822.36   Can you inspect and copy the records related to my postmarket surveillance plan?

We may, at a reasonable time and in a reasonable manner, inspect and copy any records pertaining to the conduct of postmarket surveillance that are required to be kept by this regulation. You must be able to produce records and information required by this regulation that are in the possession of others under contract with you to conduct the postmarket surveillance. Those who have signed agreements or are under contract with you must also produce the records and information upon our request. This information must be produced within 72 hours of the initiation of the inspection. We generally will redact information pertaining to individual subjects prior to copying those records, unless there are extenuating circumstances.

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