This collection is effectuated by a
guidance that provides instructions on the process for firms
seeking inclusion on an agency list of U.S. dariy firms that export
or intend to export to Chile. U.S. firms that want to be placed on
the list will send information to FDA including name and address of
the firm and the manufacturing plant, list of products presently
shipped and expected to be shipped in the future, identities of
agencies that inspect the plant, plant number and copy of last
inspection.
The burden has increased from
124 hours to 139 hours. This adjustment is a result of an increase
in the estimated number of new firms that will apply to be added to
the list, from 15 to 25 respondents.
$2,966
No
No
No
No
No
Uncollected
Domini Bean 301 796-5733
domini.bean@fda.hhs.gov
No
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.