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.