FDA Documents of Intertek USA Inc
Intertek USA Inc is an organization that has been audited by the FDA 12 times between 2002 and 2020 across all 4 sites.
Documents
FDA 483 Intertek USA Inc, San Diego | 2017
Out-of-stock
Issued on: Nov 9, 2017
Human Drug Form 483
FDA 483 Intertek USA Inc, Champaign | 2011
Out-of-stock
Issued on: Nov 18, 2011
Foods & Cosmetic Form 483
FDA 483 Intertek USA Inc, Champaign | 2010
Out-of-stock
Issued on: Sep 30, 2010
Human Drug Form 483
FDA 483 Intertek USA Inc, Champaign | 2008
Out-of-stock
Issued on: Jan 18, 2008
Human Drug Form 483
FDA 483 Intertek USA Inc, San Diego | 2004
Out-of-stock
Issued on: Apr 2, 2004
Human Drug Form 483
FDA 483 Intertek USA Inc, Champaign | 2003
Out-of-stock
Issued on: Nov 24, 2003
Human Drug Form 483
FDA 483 Intertek USA Inc, Champaign | 2002
Out-of-stock
Issued on: Oct 25, 2002
Human Drug Form 483
FDA Investigators (9)
- Norman K. Starks, FDA Investigator
- Lakecha N. Lewis, FDA Investigator
- Mohsen Rajabi Abhari, FDA Investigator
- Linda Thai, FDA Investigator
- Brian D. Nicholson, FDA Investigator
- Allen F. Hall, FDA Investigator
- Bruce H. McCullough, FDA Investigator
- Mark G. Peterson, FDA Investigator
- Susan D. Yuscius, FDA Investigator