Sanitary Transportation of Human and Animal Food

ICR 201903-0910-018

OMB: 0910-0773

Federal Form Document

Forms and Documents
Document
Name
Status
Supporting Statement A
2019-06-05
ICR Details
0910-0773 201903-0910-018
Active 201604-0910-006
HHS/FDA CFSAN
Sanitary Transportation of Human and Animal Food
Extension without change of a currently approved collection   No
Regular
Approved without change 07/08/2019
Retrieve Notice of Action (NOA) 06/05/2019
  Inventory as of this Action Requested Previously Approved
07/31/2022 36 Months From Approved 07/31/2019
1,502,260 0 3,280,611
124,848 0 375,265
3,845,407 0 3,929,115

The Food and Drug Administration is establishing requirements for shippers, carriers by motor vehicle and rail vehicle, and receivers engaged in the transportation of food, including food for animals, to use sanitary transportation practices to ensure the safety of the food they transport. This action is part of our larger effort to focus on prevention of food safety problems throughout the food chain and is part of our implementation of the Sanitary Food Transportation Act of 2005 (2005 SFTA) and the FDA Food Safety Modernization Act of 2011 (FSMA).

US Code: 21 USC 371(a) et al. Name of Law: Food, Drug, & Cosmetic Act
  
None

Not associated with rulemaking

  84 FR 5807 02/20/2019
84 FR 25816 06/04/2019
No

  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 1,502,260 3,280,611 0 0 -1,778,351 0
Annual Time Burden (Hours) 124,848 375,265 0 0 -250,417 0
Annual Cost Burden (Dollars) 3,845,407 3,929,115 0 0 -83,708 0
No
No
The information collection reflects agency adjustments. Since last OMB review we have removed one-time burdens we previously attributed to implementation of the new regulations and realization of compliance dates. Because these milestones have been met, we have removed initial burden we ascribed to associated with activities. This results in an overall decrease to the information collection by 1,778,351 responses (from 3,280,611 to 1,502,260), by 250,416 burden hours (from 375,265 to 124,849), and by $83,708 in cost adjustments.

$0
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.
06/05/2019


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