QAP modification

FDA’s Voluntary Qualified Importer Program; Guidance for Industry

⚠️ Notice: This information collection may be referencing outdated material. More recent filings for OMB 0910-0840 can be found here:

Documents and Forms

Document Name Document Type
VQIP GFI Final.pdf www.fda.gov/Food/GuidanceRegulation/FSMA/ucm253380.htm Other-Guidance for Industry

Information Collection (IC) Details

IC Title:	QAP modification	Agency IC Tracking Number:

Is this a Common Form? No		IC Status: New

Obligation to Respond: Required to Obtain or Retain Benefits

CFR Citation:

Information Collection Instruments:

Document Type	Form No.	Form Name	Instrument File	URL	Available Electronically?	Can Be Submitted Electronically?	Electronic Capability
Other-Guidance for Industry			VQIP GFI Final.pdf	http://www.fda.gov/Food/GuidanceRegulation/FSMA/ucm253380.htm	Yes	Yes	Fillable Fileable

Line of Business: Health

Subfunction: Consumer Health and Safety

Privacy Act System of Records
Title:	FR Citation:

Number of Respondents: 200	Number of Respondents for Small Entity: 0

Affected Public: Private Sector	Private Sector: Businesses or other for-profits

Percentage of Respondents Reporting Electronically: 100 %

	Requested	Program Change Due to Agency Discretion
Annual Number of Responses for this IC	200	200
Annual IC Time Burden (Hours)	3,200	3,200
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.