Regulations Under the Federal Import Milk Act

Forms and Documents

Forms and supporting documents for this ICR

Document	Type	Status	Availability
Form Form FDA 1996 Farm Inspection Report	Form and Instruction	Modified	Available
Form Form FDA 1815 Permits Granted on Certificates	Form and Instruction	Modified	Available
Form Form FDA 1993 Application for Permit	Form and Instruction	Modified	Available
Form Form FDA 1997 Score Card for Milk Plants	Form and Instruction	Modified	Available
Form Form FDA 1994 Tuberculin Test	Form and Instruction	Modified	Available
Form Form FDA 1995 Physical Examination of Cows - Report	Form and Instruction	Modified	Available
0212 FIMA SSA 2018 Ext.pdf	Supporting Statement A	Uploaded 2018-06-11	Available

IC Document Collections

Information collection document groups

IC ID	Collection	Type	Status	Form
5813	Regulations Under the Federal Import Milk Act	Form and Instruction	Modified	Farm Inspection Report
187441	Regulations Under the Federal Import Milk Act		Unchanged
187440	Regulations Under the Federal Import Milk Act	Form and Instruction	Modified	Permits Granted on Certificates
187439	Regulations Under the Federal Import Milk Act	Form and Instruction	Modified	Application for Permit
187438	Regulations Under the Federal Import Milk Act	Form and Instruction	Modified	Score Card for Milk Plants
187437	Regulations Under the Federal Import Milk Act	Form and Instruction	Modified	Tuberculin Test
187436	Regulations Under the Federal Import Milk Act	Form and Instruction	Modified	Physical Examination of Cows - Report

ICR Details

OMB Control No: 0910-0212	ICR Reference No: 201806-0910-003
Status: Historical Active	Previous ICR Reference No: 201506-0910-022
Agency/Subagency: HHS/FDA	Agency Tracking No: CFSAN
Title: Regulations Under the Federal Import Milk Act
Type of Information Collection: Extension without change of a currently approved collection	Common Form ICR:  No
Type of Review Request: Regular
OIRA Conclusion Action: Approved without change	Conclusion Date: 08/07/2018
Retrieve Notice of Action (NOA)	Date Received in OIRA: 07/05/2018
Terms of Clearance:

table that charts list comparision

	Inventory as of this Action	Requested	Previously Approved
Expiration Date	08/31/2021	36 Months From Approved	08/31/2018
Responses	410	0	410
Time Burden (Hours)	609	0	609
Cost Burden (Dollars)	0	0	0

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Abstract: The Federal Import Milk Act (FIMA) prohibits the imporation of milk and cream into the United States unless the shipper holds a valid Import Milk permit from the Food and Drug Administration. The act requires that all cows be healthy and that the dairy farm and processing plant be in good sanitary condition. The purpose of the collection is to ensure compliance with FIMA. Respondents are foreign dairy farms and plants engaged in the importation of milk and/or cream into the United States.

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Authorizing Statute(s): US Code: 21 USC 141-149 Name of Law: Federal Import Milk Act
  

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:
	83 FR 13992	04/02/2018
30-day Notice:	Federal Register Citation:	Citation Date:
	83 FR 31155	07/03/2018
Did the Agency receive public comments on this ICR? No

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Number of Information Collection (IC) in this ICR: 7

table that charts list of burden

IC Title	Form No.	Form Name
Regulations Under the Federal Import Milk Act	Form FDA 1996	Farm Inspection Report
Regulations Under the Federal Import Milk Act	Form FDA 1997	Score Card for Milk Plants
Regulations Under the Federal Import Milk Act	Form FDA 1993	Application for Permit
Regulations Under the Federal Import Milk Act
Regulations Under the Federal Import Milk Act	Form FDA 1994	Tuberculin Test
Regulations Under the Federal Import Milk Act	Form FDA 1815	Permits Granted on Certificates
Regulations Under the Federal Import Milk Act	Form FDA 1995	Physical Examination of Cows - Report

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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	410	410	0	0	0	0
Annual Time Burden (Hours)	609	609	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: $17,445

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.     No

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: 07/05/2018

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