![]() |
Code of Federal Regulations (Last Updated: July 5, 2024) |
![]() |
Title 21 - Food and Drugs |
![]() |
Chapter I - Food and Drug Administration, Department of Health and Human Services |
![]() |
SubChapter A - General |
![]() |
Part 1 - General Enforcement Regulations |
![]() |
Subpart E - Imports and Exports |
§ 1.95 - Application for authorization to relabel and recondition.
Latest version.
-
§ 1.95 Application for authorization to relabel and recondition.
Application for authorization to relabel or perform other action to bring the article into compliance with the act Federal Food, Drug, and Cosmetic Act or to render it other than a food, drug, device, or cosmetic may be filed only by the owner or consignee, and shall:
(a) Contain detailed proposals for bringing the article into compliance with the act or rendering it other than a food, drug, device, or cosmetic.
(b) Specify the time and place where such operations will be carried out and the approximate time for their completion.
[42 FR 15553, Mar. 22, 1977, as amended at 85 FR 50781, Aug. 18, 2020]