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Reportable Food (human and animal) Mandatory View
Electronic Data Collection Using MedWatchPlus Portal and Rational Questionnaire--21 CFR 310.305, 314.80, 314.98, 514.80, 600.80, 1271.350 and Part 803
OMB: 0910-0645
IC ID: 192363
OMB.report
HHS/FDA
OMB 0910-0645
ICR 201003-0910-004
IC 192363
( )
⚠️ Notice: This information collection may be referencing outdated material. More recent filings for OMB 0910-0645 can be found here:
2021-09-14 - No material or nonsubstantive change to a currently approved collection
2020-05-14 - No material or nonsubstantive change to a currently approved collection
Documents and Forms
Document Name
Document Type
Confidential 1005_Mandatory-Initial-Part_4-Adulteration_Origination_Site-040109 (2).pdf
Other-system screenshot
Confidential 1005 Mandatory-Initial-Subview Questions Explanatory Notes-040109.doc
Other-system screenshot
Confidential 1005_Mandatory-Initial-Part_3-Problem_Summary-040109.pdf
Other-system screenshot
0645 Mandatory pet screenshot 3-11-2010.doc
Other-screenshot
guidance 3-11-2010.doc
Other-guidance document
FDA 1932 Veterinary Adverse Drug Reaction, Lack of Effectiveness,
FORM FDA 1932.pdf
Form and Instruction
Information Collection (IC) Details
View Information Collection (IC)
IC Title:
Reportable Food (human and animal) Mandatory View
Agency IC Tracking Number:
Is this a Common Form?
No
IC Status:
New
Obligation to Respond:
Mandatory
CFR Citation:
Information Collection Instruments:
Document Type
Form No.
Form Name
Instrument File
URL
Available Electronically?
Can Be Submitted Electronically?
Electronic Capability
Other-system screenshot
Confidential 1005_Mandatory-Initial-Part_4-Adulteration_Origination_Site-040109 (2).pdf
Yes
Yes
Paper Only
Other-system screenshot
Confidential 1005 Mandatory-Initial-Subview Questions Explanatory Notes-040109.doc
Yes
Yes
Paper Only
Other-system screenshot
Confidential 1005_Mandatory-Initial-Part_3-Problem_Summary-040109.pdf
Yes
Yes
Paper Only
Other-screenshot
0645 Mandatory pet screenshot 3-11-2010.doc
Yes
Yes
Fillable Fileable
Form and Instruction
FDA 1932
Veterinary Adverse Drug Reaction, Lack of Effectiveness, Product Defect Report
FORM FDA 1932.pdf
Yes
No
Fillable Fileable
Other-guidance document
guidance 3-11-2010.doc
No
No
Printable Only
Federal Enterprise Architecture Business Reference Module
Line of Business:
Health
Subfunction:
Consumer Health and Safety
Privacy Act System of Records
Title:
FR Citation:
Number of Respondents:
1,200
Number of Respondents for Small Entity:
0
Affected Public:
Individuals or Households
Percentage of Respondents Reporting Electronically:
0 %
Approved
Program Change Due to New Statute
Program Change Due to Agency Discretion
Change Due to Adjustment in Agency Estimate
Change Due to Potential Violation of the PRA
Previously Approved
Annual Number of Responses for this IC
1,200
0
1,200
0
0
0
Annual IC Time Burden (Hours)
720
0
720
0
0
0
Annual IC Cost Burden (Dollars)
0
0
0
0
0
0
Documents for IC
Title
Document
Date Uploaded
No associated records found
Blank fields in records indicate information that was not collected or not collected electronically prior to July 2006.