StacksVerified U.S. regulatory reference

21 CFR §111.310

Verified against eCFR.gov as of June 20, 2026View official text on eCFR.gov
You must use adequate laboratory facilities to perform whatever testing and examinations are necessary to determine whether:
  1. (a)Components that you use meet specifications;
  2. (b)In-process specifications are met as specified in the master manufacturing record; and
  3. (c)Dietary supplements that you manufacture meet specifications.