Laboratory Approval Programs

Forms and Documents

Forms and supporting documents for this ICR

Document	Type	Status	Availability
SuptStmt 073117 FINAL.doc	Supporting Statement A	Uploaded 2017-07-31	Available
Q 15 breakout 6-29-17.pdf	Supplementary Document	Uploaded 2017-06-29	Available
AGRICULTURAL MARKETING ACT OF 1946.doc	Supplementary Document	Uploaded 2011-08-09	Available
AMS -71 GRID 6-29-17.xls	Supplementary Document	Uploaded 2017-06-29	Available

IC Document Collections

Information collection document groups

IC ID	Collection	Type	Status	Form
184032	Laboratory Approval Programs		Modified

ICR Details

OMB Control No: 0581-0251	ICR Reference No: 201706-0581-006
Status: Active	Previous ICR Reference No: 201406-0581-006
Agency/Subagency: USDA/AMS	Agency Tracking No:
Title: Laboratory Approval Programs
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: 09/05/2017
	Date Received in OIRA: 08/03/2017
Terms of Clearance:

table that charts list comparision

	Inventory as of this Action	Requested	Previously Approved
Expiration Date	09/30/2020	36 Months From Approved	09/30/2017
Responses	323	0	680
Time Burden (Hours)	4,140	0	6,290
Cost Burden (Dollars)	0	0	0

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Abstract: Agricultural Marketing Service (AMS) provides analytical testing services that facilitate marketing and allow products to obtain grade designations or meet marketing or quality standards. AMS develops and maintains laboratory approval programs as needed by the agricultural industry, to support domestic and international marketing of U.S. products.

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Authorizing Statute(s): US Code: 7 USC 1621-1627 Name of Law: Agricultural Marketing Act of 1946
  

Citations for New Statutory Requirements: None

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Associated Rulemaking Information
RIN:	Stage of Rulemaking:	Federal Register Citation:	Date:
	Not associated with rulemaking

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Federal Register Notices & Comments
60-day Notice:	Federal Register Citation:	Citation Date:
	82 FR 63	04/04/2017
30-day Notice:	Federal Register Citation:	Citation Date:
	82 FR 36114	08/03/2017
Did the Agency receive public comments on this ICR? No

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

table that charts list of burden

IC Title	Form No.	Form Name
Laboratory Approval Programs

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ICR Summary of Burden

table that charts list 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	323	680	0	-75	-282	0
Annual Time Burden (Hours)	4,140	6,290	0	148	-2,298	0
Annual Cost Burden (Dollars)	0	0	0	0	0	0

Burden increases because of Program Change due to Agency Discretion: Yes

Burden Increase Due to: Miscellaneous Actions

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

Burden Reduction Due to:

Short Statement: There is an increase in the Microbiological and Aflatoxin Programs. Program changes reflect the new Microbiological Program with 2 respondents, 10 responses and 152 hours. However, form ST2-212 was obsoleted showing a program decrease of -85 responses and -4.25 hours for program changes totaling -75 responses and +148 hours. The remaining programs decreases since the last submission are due to marketing conditions and a reduction of laboratories participating in the programs.

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Annual Cost to Federal Government: $0

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

Does this ICR request any personally identifiable information (see OMB Circular No. A-130 for an explanation of this term)? Please consult with your agency's privacy program when making this determination.     Yes

Does this ICR include a form that requires a Privacy Act Statement (see 5 U.S.C. §552a(e)(3))? Please consult with your agency's privacy program when making this determination.     No

Is this ICR related to the Affordable Care Act [Pub. L. 111-148 & 111-152]? No

Is this ICR related to the Dodd-Frank Wall Street Reform and Consumer Protection Act, [Pub. L. 111-203]? No

Is this ICR related to the American Recovery and Reinvestment Act of 2009 (ARRA)? No

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: 08/03/2017

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