Previous terms continue: At the time of the next revision/extension, FDA should report on efforts to phase-out the paper-based collection and revise burden estimates based on electronic submissions.
Inventory as of this Action
Requested
Previously Approved
11/30/2020
36 Months From Approved
4,200
0
0
3,100
0
0
0
0
0
This ICR supports an agency program by which respondents may be included on an established list of U.S. dairy firms who wish to export to foreign countries. Respondents who wish to be included on the list will voluntarily send information to FDA, including the name and address of the firm and the manufacturing plant, a list of products presently shipped and expected to be shipped in the future, and identities of agencies that inspect the plant, plant number and copy of last inspection.
This information collection reflects agency adjustments. The total annual number of responses increased from 125 to 2,000 (an increase of 1,875 responses) and the total annual burden increased from 338 to 3,100 hours (an increase of 2,762 hours).
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.