1. Regulations
  2. title 21
  3. chapter I-i1
  4. part 111
  5. subpart P
  6. § 111.610

View all text of Subpart P [§ 111.605 - § 111.610]

§ 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.

AUTHORITY: 21 U.S.C. 321, 342, 343, 371, 374, 381, 393; 42 U.S.C. 264.

SOURCE: 72 FR 34942, June 25, 2007, unless otherwise noted.

CITE AS: 21 CFR 111.610