In accordance
with the terms of 5 CFR 1320, OMB considers this package to have
been improperly submitted. The supporting statement describes a
request to approve a new form. However, no new form appears to have
been uploaded, nor is this accounted for by a change in burden.
Please review the collection and make any appropriate corrections
before resubmitting this ICR to OMB.
Inventory as of this Action
Requested
Previously Approved
08/31/2012
36 Months From Approved
02/28/2013
30
0
30
4,950
0
4,950
0
0
0
This ICR collects information used in
making a GRAS determination, and the notifier would maintain a
record of such data and information. FDA asks companies to provide
information about whether a product that they wish to market
qualifies for GRAS status.
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.