The Resource 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)

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)

Label
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)
Title
Guidance for industry, FDA staff, and FDA-accredited third parties
Title part
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)
Title variation
  • 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)
Contributor
Subject
Language
eng
Cataloging source
GPO
Government publication
federal national government publication
Index
no index present
Literary form
non fiction
Nature of contents
dictionaries
http://library.link/vocab/relatedWorkOrContributorName
  • Center for Devices and Radiological Health (U.S.)
  • Center for Biologics Evaluation and Research (U.S.)
http://library.link/vocab/subjectName
  • Medical instruments and apparatus
  • United States
Label
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)
Instantiates
Publication
Note
  • Title from PDF title screen (viewed May 24, 2012)
  • "Document issued on March 2, 2009."
  • "This document supersedes the document which was issued on September 15, 2005."
Carrier category
online resource
Carrier category code
  • cr
Carrier MARC source
rdacarrier
Color
mixed
Content category
text
Content type code
  • txt
Content type MARC source
rdacontent
Dimensions
unknown
Extent
1 online resource (10 pages)
Form of item
online
Media category
computer
Media MARC source
rdamedia
Media type code
  • c
Specific material designation
remote
Label
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)
Publication
Note
  • Title from PDF title screen (viewed May 24, 2012)
  • "Document issued on March 2, 2009."
  • "This document supersedes the document which was issued on September 15, 2005."
Carrier category
online resource
Carrier category code
  • cr
Carrier MARC source
rdacarrier
Color
mixed
Content category
text
Content type code
  • txt
Content type MARC source
rdacontent
Dimensions
unknown
Extent
1 online resource (10 pages)
Form of item
online
Media category
computer
Media MARC source
rdamedia
Media type code
  • c
Specific material designation
remote

Library Locations

    • Biddle Law LibraryBorrow it
      3400 Chestnut Street, Philadelphia, Pennsylvania, 19104, US
      39.954941 -75.193362
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