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Allegation Reporting Respondent
Electronic Submission of Allegations of Regulatory Misconduct Associated with Medical Devices
OMB: 0910-0769
IC ID: 211628
OMB.report
HHS/FDA
OMB 0910-0769
ICR 201405-0910-005
IC 211628
( )
⚠️ Notice: This information collection may be referencing outdated material. More recent filings for OMB 0910-0769 can be found here:
2023-10-12 - Extension without change of a currently approved collection
2020-10-16 - Extension without change of a currently approved collection
Documents and Forms
Document Name
Document Type
allegation report.pdf
Other-null
intro_screen_top.png
Instruction
Information Collection (IC) Details
View Information Collection (IC)
IC Title:
Allegation Reporting Respondent
Agency IC Tracking Number:
Is this a Common Form?
No
IC Status:
New
Obligation to Respond:
Voluntary
CFR Citation:
Information Collection Instruments:
Document Type
Form No.
Form Name
Instrument File
URL
Available Electronically?
Can Be Submitted Electronically?
Electronic Capability
Other-null
allegation report.pdf
Yes
Yes
Fillable Fileable
Instruction
intro_screen_top.png
No
Fillable Fileable
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:
700
Number of Respondents for Small Entity:
0
Affected Public:
Individuals or Households
Percentage of Respondents Reporting Electronically:
95 %
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
700
0
700
0
0
0
Annual IC Time Burden (Hours)
175
0
175
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.