CFR

CFR

PART 111—CURRENT GOOD MANUFACTURING PRACTICE IN MANUFACTURING, PACKAGING, LABELING, OR HOLDING OPERATIONS FOR DIETARY SUPPLEMENTS

SUBPART A—General Provisions (§111.1 to §111.5)
SUBPART B—Personnel (§111.8 to §111.14)
SUBPART C—Physical Plant and Grounds (§111.15 to §111.23)
SUBPART D—Equipment and Utensils (§111.25 to §111.35)
SUBPART E—Requirement to Establish a Production and Process Control System (§111.55 to §111.95)
SUBPART F—Production and Process Control System: Requirements for Quality Control (§111.103 to §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
SUBPART H—Production and Process Control System: Requirements for the Master Manufacturing Record (§111.205 to §111.210)
SUBPART I—Production and Process Control System: Requirements for the Batch Production Record (§111.255 to §111.260)
SUBPART J—Production and Process Control System: Requirements for Laboratory Operations (§111.303 to §111.325)
SUBPART K—Production and Process Control System: Requirements for Manufacturing Operations (§111.353 to §111.375)
SUBPART L—Production and Process Control System: Requirements for Packaging and Labeling Operations (§111.403 to §111.430)
SUBPART M—Holding and Distributing (§111.453 to §111.475)
SUBPART N—Returned Dietary Supplements (§111.503 to §111.535)
SUBPART O—Product Complaints (§111.553 to §111.570)
SUBPART P—Records and Recordkeeping (§111.605 to §111.610)

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