21 CFR Part 111 - CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PACKAGING, LABELING, OR HOLDING OPERATIONS FOR DIETARY SUPPLEMENTS
- SUBPART A — General Provisions (§§ 111.1 - 111.5)
- SUBPART B — Personnel (§§ 111.8 - 111.14)
- SUBPART C — Physical Plant and Grounds (§§ 111.15 - 111.23)
- SUBPART D — Equipment and Utensils (§§ 111.25 - 111.35)
- SUBPART E — Requirement to Establish a Production and Process Control System (§§ 111.55 - 111.95)
- SUBPART F — Production and Process Control System: Requirements for Quality Control (§§ 111.103 - 111.140)
- SUBPART G — Production and Process Control System: Requirements for Components, Packaging, and Labels and for Product That You Receive for Packaging or Labeling as a Dietary Supplement (§§ 111.153 - 111.180)
- SUBPART H — Production and Process Control System: Requirements for the Master Manufacturing Record (§§ 111.205 - 111.210)
- SUBPART I — Production and Process Control System: Requirements for the Batch Production Record (§§ 111.255 - 111.260)
- SUBPART J — Production and Process Control System: Requirements for Laboratory Operations (§§ 111.303 - 111.325)
- SUBPART K — Production and Process Control System: Requirements for Manufacturing Operations (§§ 111.353 - 111.375)
- SUBPART L — Production and Process Control System: Requirements for Packaging and Labeling Operations (§§ 111.403 - 111.430)
- SUBPART M — Holding and Distributing (§§ 111.453 - 111.475)
- SUBPART N — Returned Dietary Supplements (§§ 111.503 - 111.535)
- SUBPART O — Product Complaints (§§ 111.553 - 111.570)
- SUBPART P — Records and Recordkeeping (§§ 111.605 - 111.610)
Authority:
Source:
72 FR 34942, June 25, 2007, unless otherwise noted.
Title 21 published on 2012-04-01
no entries appear in the Federal Register after this date.
This is a list of United States Code sections, Statutes at Large, Public Laws, and Presidential Documents, which provide rulemaking authority for this CFR Part.
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