Allegation Reporting Respondent

Electronic Submission of Allegations of Regulatory Misconduct Associated with Medical Devices

⚠️ Notice: This information collection may be referencing outdated material. More recent filings for OMB 0910-0769 can be found here:

Documents and Forms

Document Name Document Type
Reporting Allegations of Regulatory Misconduct _ Allegations of Regulatory Misconduct Form.pdf Other-Allegations of Regulatory Misc
Reporting Allegations of Regulatory Misconduct - Intro Screen.pdf Instruction

Information Collection (IC) Details

IC Title:	Allegation Reporting Respondent	Agency IC Tracking Number:

Is this a Common Form? No		IC Status: Modified

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-Allegations of Regulatory Misconduct Form			Reporting Allegations of Regulatory Misconduct _ Allegations of Regulatory Misconduct Form.pdf		Yes	Yes	Fillable Fileable
Instruction			Reporting Allegations of Regulatory Misconduct - Intro Screen.pdf		No		Fillable Fileable

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	Previously Approved
Annual Number of Responses for this IC	700	700
Annual IC Time Burden (Hours)	175	175
Annual IC Cost Burden (Dollars)	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.