§111.25. What are the requirements under this subpart D for written procedures?
21 C.F.R. § 111.25
You must establish and follow written procedures for fulfilling the requirements of this subpart D, including written procedures for:
Calibrating instruments and controls that you use in manufacturing or testing a component or dietary supplement;
Calibrating, inspecting, and checking automated, mechanical, and electronic equipment; and
Maintaining, cleaning, and sanitizing, as necessary, all equipment, utensils, and any other contact surfaces that are used to manufacture, package, label, or hold components or dietary supplements.
Notes, amendments, and revision history
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.