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HHS/FDA | RIN: 0910-AF78 | Publication ID: Fall 2015 |
Title: Import Tolerances for Residues of Unapproved New Animal Drugs in Food | |
Abstract: FDA is proposing procedures by which a person may request FDA establish or amend tolerances for unapproved new animal drugs where edible portions of animals imported into the United States may contain residues of such drugs (import tolerances), or to revoke an existing import tolerance. Such import tolerances provide a basis for legally marketing food of animal origin that is imported into the United States and contains residues of unapproved new animal drugs. | |
Agency: Department of Health and Human Services(HHS) | Priority: Substantive, Nonsignificant |
RIN Status: Previously published in the Unified Agenda | Agenda Stage of Rulemaking: Final Rule Stage |
Major: No | Unfunded Mandates: No |
CFR Citation: Not Yet Determined (To search for a specific CFR, visit the Code of Federal Regulations.) | |
Legal Authority: 21 U.S.C. 342 21 U.S.C. 360b(a)(6) 21 U.S.C. 371 |
Legal Deadline:
None |
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Timetable:
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Regulatory Flexibility Analysis Required: No | Government Levels Affected: None |
Federalism: No | |
Included in the Regulatory Plan: No | |
International Impacts: This regulatory action will be likely to have international trade and investment effects, or otherwise be of international interest. | |
RIN Data Printed in the FR: No | |
Agency Contact: Joanne Kla Consumer Safety Officer Department of Health and Human Services Food and Drug Administration Center for Veterinary Medicine, 7519 Standish Place, Room 111, MPN-4, HFS-235, Rockville, MD 20855 Phone:240 402-5605 Email: joanne.kla@fda.hhs.gov |