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

ICR 201806-0910-001

OMB: 0910-0509

Federal Form Document

Forms and Documents
Document
Name
Status
Supplementary Document
2018-06-11
Justification for No Material/Nonsubstantive Change
2018-06-11
Supporting Statement A
2017-10-03
ICR Details
0910-0509 201806-0910-001
Historical Active 201708-0910-015
HHS/FDA CFSAN
Establishing and Maintaining Lists of U.S. Milk Product Manufacturers/Processors With Interest in Exporting
No material or nonsubstantive change to a currently approved collection   No
Regular
Approved without change 06/14/2018
Retrieve Notice of Action (NOA) 06/11/2018
  Inventory as of this Action Requested Previously Approved
11/30/2020 11/30/2020 11/30/2020
4,200 0 4,200
3,100 0 3,100
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 4,200 0 0 0 0
Annual Time Burden (Hours) 3,100 3,100 0 0 0 0
Annual Cost Burden (Dollars) 0 0 0 0 0 0
No
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
Domini Bean 301 796-5733 domini.bean@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.
06/11/2018


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