United States Government Publishing Office
publisher
pbl
distributor
dst
United States
Health and Human Services Department
Food and Drug Administration
author
aut
Government Organization
text
government publication
eng
GOVPUB
Executive Agency Publications
executive
2023-06-06
Health and Human Services Department
2005-01-01
monographic
harvested
born digital
13 digital object pages
HE 20.4802:IN 7
https://www.govinfo.gov/app/details/GOVPUB-HE20_4000-PURL-LPS112835
P0b002ee1bea8baf8
000639741
https://purl.fdlp.gov/GPO/LPS112835
(OCoLC)326879156
DGPO
2023-06-06
2026-07-01
GOVPUB-HE20_4000-PURL-LPS112835
machine generated
eng
fdlp
HE20_4000
GOVPUB-HE20_4000-PURL-LPS112835
PURL-LPS112835
GOVPUB
This content was harvested from online sources of the original hosting or authoring agency and may not reflect current policy. As Federal agencies add publications to their websites, or report new publications to GPO per statutory mandate (44 U.S.C. ยงยง 1710, 1902-1903), GPO ensures long-term preservation of and access to the content.
2005
PERM_INGEST_04282022
LPS112835
https://www.govinfo.gov/app/details/GOVPUB-HE20_4000-PURL-LPS112835
https://www.govinfo.gov/content/pkg/GOVPUB-HE20_4000-PURL-LPS112835/pdf/GOVPUB-HE20_4000-PURL-LPS112835.pdf
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
Inspection
Medical instruments and apparatus
United States
0499-T-02 (online)
Center for Devices and Radiological Health (U.S.)
Center for Biologics Evaluation and Research (U.S.)
mdu
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]
monographic
11 pages : digital, PDF file
HE 20.4802:IN 7
0499-T-02 (online)
text
eng
Title from PDF title page (viewed on May 19, 2009).
"Document issued on: September 15, 2005".
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.
Medical instruments and apparatus
Inspection
United States
https://purl.fdlp.gov/GPO/LPS112835
https://catalog.gpo.gov/fdlpdir/locate.jsp?ItemNumber=0499-T-02&SYS=000639741
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
Guidance for industry, FDA staff, and FDA-accredited third parties
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
Guidance for industry, FDA staff, and FDA-accredited third parties