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e-CFR data is current as of August 13, 2020

Title 21Chapter ISubchapter JPart 1002Subpart D → §1002.31


Title 21: Food and Drugs
PART 1002—RECORDS AND REPORTS
Subpart D—Manufacturers' Records


§1002.31   Preservation and inspection of records.

(a) Every manufacturer required to maintain records pursuant to this part, including records received pursuant to §1002.41, shall preserve such records for a period of 5 years from the date of the record.

(b) Upon reasonable notice by an officer or employee duly designated by the Department, manufacturers shall permit such officer or employee to inspect appropriate books, records, papers, and documents as are relevant to determining whether the manufacturer has acted or is acting in compliance with Federal standards.

(c) Upon request of the Director, Center for Devices and Radiological Health, a manufacturer of products listed in table 1 of §1002.1 shall submit to the Director, copies of the records required to be maintained by paragraph (b) of §1002.30.

[38 FR 28625, Oct. 15, 1973, as amended at 53 FR 11254, Apr. 6, 1988; 60 FR 48386, Sept. 19, 1995]

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