BLOOD BANK INSPECTION CHECKLIST

Forms and Documents

Document Name	Status

No forms / supporting documents in this ICR. Check IC Document Collections.

IC Document Collections

IC ID	Document Title	Status
113021	BLOOD BANK INSPECTION CHECKLIST Form	Migrated

ICR Details

OMB Control No: 0938-0170	ICR Reference No: 198710-0938-002
Status: Historical Active	Previous ICR Reference No: 198408-0938-014
Agency/Subagency: HHS/CMS	Agency Tracking No:
Title: BLOOD BANK INSPECTION CHECKLIST
Type of Information Collection: Revision of a currently approved collection	Common Form ICR:  No
Type of Review Request: Regular
OIRA Conclusion Action: Approved without change	Conclusion Date: 12/17/1987
	Date Received in OIRA: 10/22/1987
Terms of Clearance: Approved for use through 12/88 under the condition that the next submission is revised to incorporate new HIV testing standards outlined in the Food and Drug Administration final rulemaking entitled "General Biological Products Standards, Additional Standards for Human Blood and Blood Products, Test for Antibody to Human Deficiency Virus (HIV)."

	Inventory as of this Action	Requested	Previously Approved
Expiration Date	12/31/1988	12/31/1988	10/31/1987
Responses	1,500	0	53
Time Burden (Hours)	750	0	750
Cost Burden (Dollars)	0	0	0

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Abstract: HOSPITALS AND CLINICAL LABORATORI PARTICIPATING IN MEDICARE MUST BE APPROVED BY THE HEALTH CARE FINANCING ADMINISTRATION (HCFA) FOR COMPLIANCE WITH HEALTH AND SAFETY STANDARDS. AS PART OF THE APPROVAL PROCESS, EACH HOSPITAL OR LABORATO IS SURVEYED BY A STATE AGENCY UNDER AN AGREEMENT WITH HCFA TO DETERMIN WHETHER THE HOSPITAL OR LABORATORY MEETS FEDERAL STANDARDS.

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Authorizing Statute(s): None

Citations for New Statutory Requirements: None

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Associated Rulemaking Information
RIN:	Stage of Rulemaking:	Federal Register Citation:	Date:

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Federal Register Notices & Comments

Did the Agency receive public comments on this ICR? No

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Number of Information Collection (IC) in this ICR: 1

IC Title	Form No.	Form Name
BLOOD BANK INSPECTION CHECKLIST	HCFA-282

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ICR Summary of Burden

	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	1,500	53	0	1,447	0	0
Annual Time Burden (Hours)	750	750	0	0	0	0
Annual Cost Burden (Dollars)	0	0	0	0	0	0

Burden increases because of Program Change due to Agency Discretion: No

Burden Increase Due to:

Burden decreases because of Program Change due to Agency Discretion: No

Burden Reduction Due to:

Short Statement:

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Annual Cost to Federal Government: $0

Does this IC contain surveys, censuses, or employ statistical methods? No

Is the Supporting Statement intended to be a Privacy Impact Assessment required by the E-Government Act of 2002? No

Is this ICR related to the Affordable Care Act [Pub. L. 111-148 & 111-152]? Uncollected

Is this ICR related to the Dodd-Frank Wall Street Reform and Consumer Protection Act, [Pub. L. 111-203]? Uncollected

Is this ICR related to the American Recovery and Reinvestment Act of 2009 (ARRA)? Uncollected

Is this ICR related to the Pandemic Response? Uncollected

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Common Form ICR:  No

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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:

(a) It is necessary for the proper performance of agency functions;

(b) It avoids unnecessary duplication;

(c) It reduces burden on small entities;

(d) It uses plain, coherent, and unambiguous language that is understandable to respondents;

(e) Its implementation will be consistent and compatible with current reporting and recordkeeping practices;

(f) It indicates the retention periods for recordkeeping requirements;

(g) It informs respondents of the information called for under 5 CFR 1320.8 (b)(3) about:

(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;

(h) It was developed by an office that has planned and allocated resources for the efficient and effective management and use of the information to be collected.

(i) It uses effective and efficient statistical survey methodology (if applicable); and

(j) It makes appropriate use of information technology.

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.

Certification Date: 10/22/1987

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