Establishing and Maintaining Lists of U.S. Milk Product Manufacturers/Processors With Interest in Exporting

ICR 201708-0910-015

OMB: 0910-0509

Federal Form Document

Forms and Documents
Document
Name
Status
Supporting Statement A
2017-10-03
ICR Details
0910-0509 201708-0910-015
Historical Active 201605-0910-016
HHS/FDA CFSAN
Establishing and Maintaining Lists of U.S. Milk Product Manufacturers/Processors With Interest in Exporting
Reinstatement with change of a previously approved collection   No
Regular
Approved without change 11/03/2017
Retrieve Notice of Action (NOA) 10/04/2017
Previous terms continue: At the time of the next revision/extension, FDA should report on efforts to phase-out the paper-based collection and revise burden estimates based on electronic submissions.
  Inventory as of this Action Requested Previously Approved
11/30/2020 36 Months From Approved
4,200 0 0
3,100 0 0
0 0 0

This ICR supports an agency program by which respondents may be included on an established list of U.S. dairy firms who wish to export to foreign countries. Respondents who wish to be included on the list will voluntarily send information to FDA, including the name and address of the firm and the manufacturing plant, a list of products presently shipped and expected to be shipped in the future, and identities of agencies that inspect the plant, plant number and copy of last inspection.

US Code: 21 USC 301 et. seq. Name of Law: FFDCA
  
None

Not associated with rulemaking

  82 FR 27485 06/15/2017
82 FR 46074 10/03/2017
Yes

3
IC Title Form No. Form Name
New Written Request to be Placed on the List
Biennial Update of Infomation
Occasional Update of Information

  Total Approved Previously Approved Change Due to New Statute Change Due to Agency Discretion Change Due to Adjustment in Estimate Change Due to Potential Violation of the PRA
Annual Number of Responses 4,200 0 0 300 3,900 0
Annual Time Burden (Hours) 3,100 0 0 338 2,762 0
Annual Cost Burden (Dollars) 0 0 0 0 0 0
Yes
Miscellaneous Actions
No
This information collection reflects agency adjustments. The total annual number of responses increased from 125 to 2,000 (an increase of 1,875 responses) and the total annual burden increased from 338 to 3,100 hours (an increase of 2,762 hours).

$6,316
No
    No
    No
No
No
No
Uncollected
Ila Mizrachi 301 796-7726 ila.mizrachi@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.
10/04/2017


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