FDA Documents of Teva Czech Industries s.r.o.
Teva Czech Industries s.r.o. is an organization that has been audited by the FDA 11 times between 2001 and 2022 across all 4 sites.
Documents
FDA 483 Teva Czech Industries s.r.o., Opava 9 | 2017
Out-of-stock
Issued on: Mar 24, 2017
Human Drug Form 483
FDA 483 Teva Czech Industries s.r.o., Opava-Komarov | 2011
Out-of-stock
Issued on: Sep 22, 2011
Human Drug Form 483
FDA 483 Teva Czech Industries s.r.o., Opava-Komarov | 2008
Out-of-stock
Issued on: Sep 18, 2008
Human Drug Form 483
FDA 483 Teva Czech Industries s.r.o., Opava-Komarov | 2006
Out-of-stock
Issued on: Feb 8, 2006
Human Drug Form 483
FDA 483 Teva Czech Industries s.r.o., Opava-Komarov | 2002
Out-of-stock
Issued on: Mar 29, 2002
Human Drug Form 483
FDA 483 Teva Czech Industries s.r.o., Opava-Komarov | 2001
Out-of-stock
Issued on: Feb 2, 2001
Human Drug Form 483
FDA Investigators(11)
- MRA McCulloughJ, FDA Investigator
- MRA DavisM, FDA Investigator
- Laurimer Kuilan-Torres, FDA Investigator
- Christina A. Miller, FDA Investigator
- Marvin D. Jones, FDA Investigator
- Maya M. Davis, FDA Investigator
- Charles Cote, FDA Investigator
- Margaret M. Annes, FDA Investigator
- Cynthia J. Lee, FDA Investigator
- Azza Talaat, FDA Investigator
- Donald L. Lech, FDA Investigator