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e-CFR data is current as of January 19, 2021 |
Title 21 → Chapter I → Subchapter B → Part 111 → Subpart P → §111.610 |
Title 21: Food and Drugs
PART 111—CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PACKAGING, LABELING, OR HOLDING OPERATIONS FOR DIETARY SUPPLEMENTS
Subpart P—Records and Recordkeeping
§111.610 What records must be made available to FDA?
(a) You must have all records required under this part, or copies of such records, readily available during the retention period for inspection and copying by FDA when requested.
(b) If you use reduction techniques, such as microfilming, you must make suitable reader and photocopying equipment readily available to FDA.