[Federal Register: December 22, 1999 (Volume 64, Number 245)] [Notices] [Page 71792-71793] From the Federal Register Online via GPO Access [wais.access.gpo.gov] [DOCID:fr22de99-99] ======================================================================= ----------------------------------------------------------------------- DEPARTMENT OF HEALTH AND HUMAN SERVICES Food and Drug Administration [Docket No. 99F-5321] United States Department of Agriculture, Food Safety and Inspection Service; Filing of Food Additive Petition AGENCY: Food and Drug Administration, HHS. ACTION: Notice. ----------------------------------------------------------------------- SUMMARY: The Food and Drug Administration (FDA) is announcing that the United States Department of Agriculture, Food Safety and Inspection Service (USDA/FSIS) has filed a petition proposing that the food additive regulations be amended to provide for the safe use of a 4.5 kiloGray (kGy) maximum dose of ionizing radiation to treat unrefrigerated (as well as refrigerated) uncooked meat, meat products, and certain meat food products to reduce levels of foodborne pathogens and extend shelf-life. [[Page 71793]] FOR FURTHER INFORMATION CONTACT: Rudaina H. Alrefai, Center for Food Safety and Applied Nutrition (HFS-206), Food and Drug Administration, 200 C St. SW., Washington, DC 20204, 202-418-3034. SUPPLEMENTARY INFORMATION: Under the Federal Food, Drug, and Cosmetic Act (sec. 409(b)(5) (21 U.S.C. 348(b)(5))), notice is given that a food additive petition (FAP 9M4695) has been filed by the USDA/FSIS, 300 12th St. SW., rm. 112, Washington, DC 20250. The petition proposes that the food additive regulations in Sec. 179.26(b) Ionizing radiation for the treatment of food (21 CFR 179.26(b)) be amended to provide for the safe use of a 4.5 kGy maximum dose of ionizing radiation to treat unrefrigerated (as well as refrigerated) uncooked meat, meat products, and certain meat food products to reduce levels of foodborne pathogens and extend shelf-life. The current regulations in Sec. 179.26(b) provide for the use of a maximum dose of 4.5 kGy to treat refrigerated products only. The agency has determined under 21 CFR 25.32(j) that this action is of a type that does not individually or cumulatively have a significant effect on the human environment. Therefore, neither an environmental assessment nor an environmental impact statement is required. Dated: December 3, 1999. Alan M. Rulis, Director, Office of Premarket Approval, Center for Food Safety and Applied Nutrition. [FR Doc. 99-33093 Filed 12-21-99; 8:45 am] BILLING CODE 4160-01-F