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Regulations last checked for updates: Nov 21, 2024
Title 21 - Food and Drugs last revised: Nov 19, 2024
All Titles
Title 21
Chapter I
Part 607 - PART 607—ESTABLISHMENT REGISTRATION AND PRODUCT LISTING FOR MANUFACTURERS OF HUMAN BLOOD AND BLOOD PRODUCTS AND LICENSED DEVICES
Subpart A [§ 607.1 - § 607.7] - Subpart A—General Provisions
Subpart B [§ 607.20 - § 607.39] - Subpart B—Procedures for Domestic Blood Product Establishments
Subpart C [§ 607.40 - § 607.40] - Subpart C—Procedures for Foreign Blood Product Establishments
Subpart D [§ 607.65 - § 607.65] - Subpart D—Exemptions
Subpart E [§ 607.80 - § 607.80] - Subpart E—Establishment Registration and Product Listing Of Licensed Devices
authority:
21 U.S.C. 321
,
331
,
351
,
352
,
355
,
360
,
371
,
374
,
381
,
393
;
42 U.S.C. 262
,
264
,
271
source:
40 FR 52788, Nov. 12, 1975, unless otherwise noted.
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