Research Catalog

Title

Requests for inspection by an accredited person under the Inspection by Accredited Persons Program authorized by Section 201 of the Medical Device User Fee and Modernization Act of 2002.

Publication

[Rockville, MD] : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Devices and Radiological Health : Center for Biologics Evaluation and Research, [2005]

Details

Additional Authors

• Center for Devices and Radiological Health (U.S.)
• Center for Biologics Evaluation and Research (U.S.)

Description

11 pages : digital, PDF file

Alternative Title

Guidance for industry, FDA staff, and FDA-accredited third parties

Subject

• Medical instruments and apparatus > Inspection > United States

Note

• Title from PDF title page (viewed on May 19, 2009).
• "Document issued on: September 15, 2005".

System Details (note)

• Mode of access: Internet at the FDA CBER web site. Address as of 5/19/09: http://www.fda.gov/cdrh/comp/guidance/1532.pdf ; current access is available via PURL.

Call Number

GPO Internet HE 20.4802:IN 7

OCLC

marcive326879156

Title

Requests for inspection by an accredited person under the Inspection by Accredited Persons Program authorized by Section 201 of the Medical Device User Fee and Modernization Act of 2002.

Publisher

[Rockville, MD] : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Devices and Radiological Health : Center for Biologics Evaluation and Research, [2005]

Type of Content

text

Type of Medium

computer

Type of Carrier

online resource

System Details

Mode of access: Internet at the FDA CBER web site. Address as of 5/19/09: http://www.fda.gov/cdrh/comp/guidance/1532.pdf ; current access is available via PURL.

Connect to:

https://purl.fdlp.gov/GPO/LPS112835

Added Author

Center for Devices and Radiological Health (U.S.)

Center for Biologics Evaluation and Research (U.S.)

Gpo Item No.

0499-T-02 (online)

Sudoc No.

HE 20.4802:IN 7