Part 226—Current Good Manufacturing Practice for Type a Medicated Articles

Subparts

• Subpart A
  Subpart A—General Provisions Sections 226.1–226.10
• Subpart B
  Subpart B—Construction and Maintenance of Facilities and Equipment Sections 226.20–226.30
• Subpart C
  Subpart C—Product Quality Control Sections 226.40–226.58
• Subpart D
  Subpart D—Packaging and Labeling Section 226.80
• Subpart E
  Subpart E—Records and Reports Sections 226.102–226.115