---
kind: "section"
citation: "21 C.F.R. § 111.610"
title: "21"
number: "111.610"
heading: "What records must be made available to FDA?"
url: "https://uscodex.org/cfr/21/111.610"
---

# §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.

## Notes

### Authority

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

### Source

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