§ 111.610. What records must be made available to FDA?
50 words·~1 min read·
/us/cfr/t21/s§ 111.610·A research copy — for the controlling text, always check the official state or federal source. Not legal advice.
(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.