0910-AE96 0910-AB26 200310 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 Revisions to Labeling and Storage Requirements for Blood and Blood Components, Including Source Plasma Other Significant Previously Published in The Unified Agenda Proposed Rule Stage Undetermined No 21 CFR 600 21 CFR 601 21 CFR 606 21 CFR 607 21 CFR 610 21 CFR 630 21 CFR 640 21 CFR 660 21 CFR 680 21 USC 321 21 USC 331 21 USC 351 to 353 21 USC 355 21 USC 360 21 USC 371 21 USC 374 42 USC 216 42 USC 262 42 USC 263 42 USC 263a 42 USC 264 No NPRM 07/30/2003 68 FR 44678 Correction Notice 10/27/2003 68 FR 61172 NPRM Comment Period End 10/30/2003 Final Action 10/00/2004 No Businesses None No NA Not Collected 0910-AB76 Related to