The information collected would be
required by FDA in order to respond to notices claiming
certification for batches of lakes as required by section 721 of
the FD&C Act and proposed revision of 21 CFR part 80. FDA
activity would include review of the notice and issuance of an
acceptance or rejection of the notice. Respondents are
manufacturers and repackers of lakes.
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.