0910-AF71 200710 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 Medical Devices; Current Good Manufacturing Practice (CGMP) Final Rule; Quality Systems Regulations Routine and Frequent Previously Published in The Unified Agenda Completed Actions No No Completion of a Section 610 Review 21 CFR 808 21 CFR 812 21 CFR 820 5 USC 610 No Begin Review of Current Regulation 01/05/2006 End Review 07/31/2007 No None No Yes Not Collected Madhusoodana Nambiar 0910 Food and Drug Administration FDA 301 796-5837 301 847-8145 madhusoodana.nambiar@fda.hhs.gov Center for Devices and Radiological Health, WO 66, Room 5518, 10903 New Hampshire Avenue, Silver Spring MD 20993