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Title 21 Part 111 → Subpart D → §111.25

Title 21 → Chapter I → Subchapter B → Part 111 → Subpart D → §111.25

Electronic Code of Federal Regulations e-CFR

Title 21 Part 111 → Subpart D → §111.25

e-CFR data is current as of February 14, 2020

Title 21Chapter ISubchapter BPart 111Subpart D → §111.25


Title 21: Food and Drugs
PART 111—CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PACKAGING, LABELING, OR HOLDING OPERATIONS FOR DIETARY SUPPLEMENTS
Subpart D—Equipment and Utensils


§111.25   What are the requirements under this subpart D for written procedures?

You must establish and follow written procedures for fulfilling the requirements of this subpart D, including written procedures for:

(a) Calibrating instruments and controls that you use in manufacturing or testing a component or dietary supplement;

(b) Calibrating, inspecting, and checking automated, mechanical, and electronic equipment; and

(c) 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.