21 CFR
Part 225 Current Good Manufacturing Practice for Medicated Feeds
Subpart A - General Provisions
Subpart B - Construction and Maintenance of Facilities and Equipment
- § 225.20 Buildings 77 × 483
- § 225.30 Equipment 75 × 483
- § 225.35 Use of work areas, equipment, and storage areas for other manufacturing and storage purpose
Subpart C - Product Quality Control
- § 225.42 Components 208 × 483
- § 225.58 Laboratory controls 133 × 483
- § 225.65 Equipment cleanout procedures 46 × 483
Subpart D - Packaging and Labeling
- § 225.80 Labeling 34 × 483
Subpart E - Records and Reports
- § 225.102 Master record file and production records 138 × 483
- § 225.110 Distribution records 3 × 483
- § 225.115 Complaint files 10 × 483
Subpart F - Facilities and Equipment
- § 225.120 Buildings and grounds 63 × 483
- § 225.130 Equipment 37 × 483
- § 225.135 Work and storage areas 2 × 483
Subpart G - Product Quality Assurance
- § 225.142 Components 115 × 483
- § 225.158 Laboratory assays 22 × 483
- § 225.165 Equipment cleanout procedures 50 × 483
Subpart H - Labeling
- § 225.180 Labeling 55 × 483