Regulatory Counsel

0910-AI05 202310 The Regulatory Plan and the Unified Agenda of Federal Regulatory and Deregulatory Actions 0910 Food and Drug Administration FDA 0900 Department of Health and Human Services HHS Administrative Detention of Tobacco Products

FDA is proposing a regulation to establish requirements for the administrative detention of tobacco products. This proposed rule, when finalized, would allow FDA to administratively detain tobacco products encountered during inspections of manufacturers or other establishments that manufacture, process, pack, or hold tobacco products that an authorized FDA representative conducting the inspection has reason to believe are adulterated or misbranded. The intent of administrative detention is to protect public health by preventing the distribution or use of tobacco products encountered during inspections that are believed to be adulterated or misbranded until FDA has had time to consider the appropriate action to take and, where appropriate, to initiate legal action.

]]> Other Significant Previously Published in The Unified Agenda Proposed Rule Stage No No 21 CFR 1100 21 U.S.C. 334 21 U.S.C. 371 No NPRM 10/00/2024 Yes Businesses None No Yes No Quynh Nguyen Regulatory Counsel 0910 Food and Drug Administration FDA 877 287-1373 ctpregulations@fda.hhs.gov Center for Tobacco Products, 10903 New Hampshire Avenue, Document Control Center, Building 71, Room G335, Silver Spring MD 20993 Laura Chilaka Regulatory Counsel 0910 Food and Drug Administration FDA 240 402-2236 ctpregulations@fda.hhs.gov 10903 New Hampshire Avenue, Center for Tobacco Products, Document Control Center, Building 71, Room G335, Silver Spring MD 20993