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
Section 801(e)(4) of the act provides that persons exporting certain FDA-regulated products may request FDA to certify that the products meet the requirements of Sections 801(e) or 802 of the FD&C Act, or other requirements of the act. This section of the law requires FDA to issue export certificates within 20 days of receipt of the request and to charge firms up to $175 for the certificates.
On behalf of this Federal agency, I certify that the collection of information encompassed by this request complies with 5 CFR 1320.9 and the related provisions of 5 CFR 1320.8(b)(3).
The following is a summary of the topics, regarding the proposed collection of information, that the certification covers:
(i) Why the information is being collected;
(ii) Use of information;
(iii) Burden estimate;
(iv) Nature of response (voluntary, required for a benefit, or mandatory);
(v) Nature and extent of confidentiality; and
(vi) Need to display currently valid OMB control number;
If you are unable to certify compliance with any of these provisions, identify the item by leaving the box unchecked and explain the reason in the Supporting Statement.