Guidance for industry, FDA staff, and FDA-accredited third parties. Manufacturer's notification of the intent to use accredited person under the accredited person inspection program authorized by Section 228 of the Food and Drug Administration Amendments Act of 2007 (FDAAA).

Format:

Book

Government document

Contributor:

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

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

Language:

English

Subjects (All):

United States. Food and Drug Administration.

United States.

Medical instruments and apparatus--Government policy--United States.

Medical instruments and apparatus.

Medical instruments and apparatus--Government policy.

Physical Description:

1 online resource (10 pages)

Other Title:

Guidance for industry, Food and Drug Administration staff, and Food and Drug Administration accredited third parties. Manufacturer's notification of the intent to use accredited person under the accredited person inspection program authorized by Section 228 of the Food and Drug Administration Amendments Act of 2007 (FDAAA)

Manufacturer's notification of the intent to use accredited person under the accredited person inspection program authorized by Section 228 of the Food and Drug Administration Amendments Act of 2007 (FDAAA)

Place of Publication:

[Rockville, Md.] : U.S. Dept. of Health and Human Services, Food and Drug Administration, Center for Devices and Radiological Health ; [Bethesda, Md.] : Center for Biologics Evaluation and Research, [2009]

Notes:

Title from PDF title screen (viewed May 24, 2012).

"Document issued on March 2, 2009."

"This document supercedes the document which was issued on September 15, 2005."

OCLC:

794684490