UNTIL IT IS
REPLACED BY THE FDA 1900. SINCE FDA HAS DECIDED TO CONTIN USE OF
THE FDA 1800, THERE WILL NO LONGER BE A NEED FOR THE FDA 1900.
CONSEQUENTLY, BURDEN ASSOCIATED WITH THE FDA 1900 HAS BEEN DELETED
FROM THE 1984 INFOMATION COLLECTION BUDGET. FDA SHALL INCREASE THE
BURDEN ESTIMATES ASSOCIATED WITH THE FDA 1800 TO REFLECT THE BURDEN
ASSOCIATED WITH THE ASSAY REQUIREMENT IF AND WHEN IT IS REQUIRED BY
TH FINALIZED A-40.
Inventory as of this Action
Requested
Previously Approved
09/30/1984
09/30/1984
09/30/1982
10,000
0
5,550
20,000
0
11,100
0
0
0
PROVIDES THE AGENCY WITH THE
INFORMATION REQUIRED TO AID IN THE ASSURANCE THAT MEDICATED FEEDS
WILL BE MANUFACTURED IN ACCORDANCE WITH THE FD&C ACT AND ITS
REGULATIONS CONCERNING PROPER MANUFACTURING AND LABELING OF NEW
ANIMAL DRUG PREMIXES.
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.