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Code of Federal Regulations (Last Updated: November 8, 2024) |
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Title 21 - Food and Drugs |
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Chapter I - Food and Drug Administration, Department of Health and Human Services |
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SubChapter C - Drugs: General |
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Part 225 - Current Good Manufacturing Practice for Medicated Feeds |
| Subpart A - General Provisions |
| § 225.1 - Current good manufacturing practice. |
| § 225.10 - Personnel. |
| Subpart B - Construction and Maintenance of Facilities and Equipment |
| § 225.20 - Buildings. |
| § 225.30 - Equipment. |
| § 225.35 - Use of work areas, equipment, and storage areas for other manufacturing and storage purpose. |
| Subpart C - Product Quality Control |
| § 225.42 - Components. |
| § 225.58 - Laboratory controls. |
| § 225.65 - Equipment cleanout procedures. |
| Subpart D - Packaging and Labeling |
| § 225.80 - Labeling. |
| Subpart E - Records and Reports |
| § 225.102 - Master record file and production records. |
| § 225.110 - Distribution records. |
| § 225.115 - Complaint files. |
| Subpart F - Facilities and Equipment |
| § 225.120 - Buildings and grounds. |
| § 225.130 - Equipment. |
| § 225.135 - Work and storage areas. |
| Subpart G - Product Quality Assurance |
| § 225.142 - Components. |
| § 225.158 - Laboratory assays. |
| § 225.165 - Equipment cleanout procedures. |
| Subpart H - Labeling |
| § 225.180 - Labeling. |
| Subpart I - Records |
| § 225.202 - Formula, production, and distribution records. |