Application for authorization to relabel and recondition

Imports and Electronic Import Entries

Documents and Forms

Document Name Document Type
Form FDA 766 Application for authorization to relabel and recondition Form and Instruction
FDA 766 APPLICATION FOR AUTHORIZATION TO RELABEL OR TO PERFORM O Form FDA 766 App to relabel Exp JUL 2020.pdf Form and Instruction
FDA 766 APPLICATION FOR AUTHORIZATION TO RELABEL OR RECONDITION 0046 Changes to FDA 766 Nov 2020.pdf Form and Instruction

Information Collection (IC) Details

IC Title:	Application for authorization to relabel and recondition	Agency IC Tracking Number:

Is this a Common Form? No		IC Status: Unchanged

Obligation to Respond: Required to Obtain or Retain Benefits

CFR Citation: 21 CFR 1.95

Information Collection Instruments:

Document Type	Form No.	Form Name	Instrument File	URL	Available Electronically?	Can Be Submitted Electronically?	Electronic Capability
Form and Instruction	FDA 766	APPLICATION FOR AUTHORIZATION TO RELABEL OR TO PERFORM OTHER ACTION OF THE FEDERAL FOOD, DRUG, AND COSMETIC ACT AND OTHER RELATED ACTS	Form FDA 766 App to relabel Exp JUL 2020.pdf		Yes	Yes	Fillable Fileable
Form and Instruction	FDA 766	APPLICATION FOR AUTHORIZATION TO RELABEL OR RECONDITION NON-COMPLIANT ARTICLES	0046 Changes to FDA 766 Nov 2020.pdf		Yes	Yes	Fillable Fileable

Line of Business: Health

Subfunction: Consumer Health and Safety

Privacy Act System of Records
Title:	FR Citation:

Number of Respondents: 324	Number of Respondents for Small Entity: 0

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

Percentage of Respondents Reporting Electronically: 95 %

	Requested	Previously Approved
Annual Number of Responses for this IC	324	324
Annual IC Time Burden (Hours)	81	81
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.