REPORTING REQUIREMENTS APPLICABLE TO THE MANUFACTURE OF BLOOD GROUPING SERUM

ICR 198302-0910-003

OMB: 0910-0137

Federal Form Document

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ICR Details
0910-0137 198302-0910-003
Historical Active 198110-0910-008
HHS/FDA
REPORTING REQUIREMENTS APPLICABLE TO THE MANUFACTURE OF BLOOD GROUPING SERUM
Revision of a currently approved collection   No
Regular
Approved without change 04/11/1983
Retrieve Notice of Action (NOA) 02/25/1983
APPROVAL HAS BEEN EXTENDED WITH THE UNDERSTANDING THAT THE REGULATION CONTAINING THE RECORDKEEPING REQUIREMENT WILL BE PROPOSED FOR RECISSIO
  Inventory as of this Action Requested Previously Approved
07/31/1984 07/31/1984 03/31/1983
1,935 0 3,575
15,480 0 28,600
0 0 0

THIS REQUIRES THE REPORTING OF INFORMATION ON EACH MANUFACTURED LOT OF BLOOD GROUPING SERUM FOR AGENCY TESTING, EVALUATION, AND OFFICIAL RELEASE OF THE LOT PRIOR TO DISTRIBUTION OF THE LOT BY THE MANUFACTURE

None
None


No

1
IC Title Form No. Form Name
REPORTING REQUIREMENTS APPLICABLE TO THE MANUFACTURE OF BLOOD GROUPING SERUM

  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 1,935 3,575 0 0 -1,640 0
Annual Time Burden (Hours) 15,480 28,600 0 0 -13,120 0
Annual Cost Burden (Dollars) 0 0 0 0 0 0
No
No

$0
No
No
Uncollected
Uncollected
Uncollected
Uncollected

  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.
02/25/1983


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