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Regulations last checked for updates: Jan 10, 2026
Title 21 - Food and Drugs last revised: Dec 18, 2026
All Titles
Title 21
Chapter I
Part 213 - PART 213—CURRENT GOOD MANUFACTURING PRACTICE FOR MEDICAL GASES
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
authority:
21 U.S.C. 321
,
351
,
352
,
353
,
355
,
360b
,
360ddd
,
360ddd
-1,
371
,
374
source:
89 FR 51770, June 18, 2024, unless otherwise noted.
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