View ICR - OIRA Conclusion



0910-0498 201010-0910-002
Historical Inactive 200903-0910-006
HHS/FDA
Export Certificates for FDA Regulated Products under U.S.C. Sections 801(e) and 802
Extension without change of a currently approved collection   No
Regular
Improperly submitted and continue 12/08/2010
10/12/2010
Under the terms of 5 CFR 1320, OMB considers this collection to have been improperly submitted. FDA has failed to meet the previously established terms of clearance. The Agency has neither made this collection available electronically, nor has it submitted to OMB a timeline for coming into compliance with GEPA. Please resubmit with a detailed timeline for GEPA compliance.
  Inventory as of this Action Requested Previously Approved
10/31/2010 36 Months From Approved 12/31/2010
24,272 0 24,272
39,333 0 39,333
0 0 0