Request for Qualitative Feedback Generic Clearance About FDA . gov Web Site Customers

Generic Clearance for the Collection of Qualitative Feedback on FDA Service Delivery

⚠️ Notice: This information collection may be referencing outdated material. More recent filings for OMB 0910-0697 can be found here:

Documents and Forms

Document Name Document Type
Appendix A- FDA External Focus Group Moderator Guide.doc Other-Survey
Justification Memo - FDA.gov Web Site Customer service.doc Justification Memo - FDA IC Document

Information Collection (IC) Details

IC Title:	Request for Qualitative Feedback Generic Clearance About FDA . gov Web Site Customers	Agency IC Tracking Number:

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-Survey			Appendix A- FDA External Focus Group Moderator Guide.doc		Yes	No	Printable Only

Line of Business: Health

Subfunction: Health Care Services

Privacy Act System of Records
Title:	FR Citation:

Number of Respondents: 206	Number of Respondents for Small Entity: 0

Affected Public: Private Sector	Private Sector: Not-for-profit institutions

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	206	0	0	0	0	0
Annual IC Time Burden (Hours)	206	0	0	0	0	0
Annual IC Cost Burden (Dollars)	0	0	0	0	0	0

Documents for IC

Title	Document	Date Uploaded
Justification Memo - FDA	Justification Memo - FDA.gov Web Site Customer service.doc	07/30/2012

Blank fields in records indicate information that was not collected or not collected electronically prior to July 2006.