View Generic ICR - OIRA Conclusion



0910-0697 202206-0910-016
Historical Active 202011-0910-002
HHS/FDA Generic
Generic Clearance for the Collection of Qualitative Feedback on Food and Drug Administration Service Delivery
No material or nonsubstantive change to a currently approved collection   No
Regular
Approved without change 07/05/2022
Retrieve Notice of Action (NOA) 06/30/2022
Previous terms continue: OMB approves this collection for a period of three years. To request approval of information collections under this generic approval, the agency must do the following: 1) Unless an agency is using multiple modes of collection (e.g., paper forms and electronic submissions), provide a Generic Clearance Submission Template for each Instrument; 2) If the agency is using multiple modes of collection (e.g., paper forms and electronic submissions), the same Generic Clearance Submission Template may be used for both instruments; 3) each Generic Clearance Submission Template must be uploaded as a Supplementary document using a naming convention that allows the public to identify the associated instrument; 4) submit no more than five Generic Submission Templates with each request.
  Inventory as of this Action Requested Previously Approved
12/31/2023 12/31/2023 12/31/2023
15,752 0 15,752
8,491 0 8,491
0 0 0