CFR section
21 CFR 225.142: Components
PART 225-CURRENT GOOD MANUFACTURING PRACTICE FOR MEDICATED FEEDS · Subpart G-Product Quality Assurance
Key facts
| Citation | 21 CFR 225.142 |
|---|---|
| Section | Components |
| Part | PART 225-CURRENT GOOD MANUFACTURING PRACTICE FOR MEDICATED FEEDS |
| Subpart | Subpart G-Product Quality Assurance |
| Subchapter | 21 CFR C Drugs General |
| Product types cited | Drugs, Food/Cosmetics, General, Veterinary |
| Regulation text (excerpt) | Adequate procedures shall be established and maintained for the identification, storage, and inventory control (receipt and use) of all Type A medicated articles and Type B medicated feeds intended for use in the manufacture of medicated feeds to aid in assuring the identity, strength, quality, and purity of these drug sources. Packaged Type A medicated articles and Type B medicated feeds shall be stored in designated areas in their original closed containers. Bulk Type A medicated articles and… |
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About CFR sections cited by the FDA
Title 21 of the Code of Federal Regulations contains the FDA's regulations, including current good manufacturing practice and quality system requirements that inspections cite.