Code of Federal Regulations > Title 21 > Chapter I > Part 213 - PART 213—CURRENT GOOD MANUFACTURING PRACTICE FOR MEDICAL GASES

U.S. Code of Federal Regulations

Regulations most recently checked for updates: Jan 21, 2026

Subpart A [§ 213.1 - § 213.3] - Subpart A—General Provisions

Subpart B [§ 213.22 - § 213.34] - Subpart B—Organization and Personnel

Subpart C [§ 213.42 - § 213.42] - Subpart C—Buildings and Facilities

Subpart D [§ 213.63 - § 213.68] - Subpart D—Equipment

Subpart E [§ 213.80 - § 213.94] - Subpart E—Control of Incoming Designated Medical Gas, Components, and Medical Gas Containers and Closures

Subpart F [§ 213.100 - § 213.110] - Subpart F—Production and Process Controls

Subpart G [§ 213.122 - § 213.130] - Subpart G—Packaging and Labeling Control

Subpart H [§ 213.150 - § 213.150] - Subpart H—Holding and Distribution

Subpart I [§ 213.160 - § 213.166] - Subpart I—Laboratory Controls

Subpart J [§ 213.180 - § 213.198] - Subpart J—Records

Subpart K [§ 213.204 - § 213.208] - Subpart K—Returned and Salvaged Medical Gases