THE INFORMATION PROVIDED IS NECESSARY
FOR AGENCY REVIEW TO DETERMINE AUTHORIZATION TO RELABEL OR
RECONDITION ADULTERATED OR MISBRANDED IMPORTED ARTICLES. THE
IMPORTER SUPPLIES THIS INFORMATION TO FDA AT T PORT OF ENTRY FOR
THE ADULTERATED OR MISBRANDED ARTICLE. IF THE INFORMATION IS NOT
PROVIDED, THE ARTICLE IS REFUSED ADMISSION AND MUST BE EXPORTED
WITHIN 90 DAYS OR DESTROYED.
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.