FDA Documents of Vimta Labs Ltd.
Vimta Labs Ltd. is an organization that has been audited by the FDA 13 times between 2005 and 2019 across all 4 sites.
Documents
FDA 483 Vimta Labs Ltd., Hyderabad | 2019
Out-of-stock
Issued on: Dec 18, 2019
Human Drug Form 483
FDA 483 Vimta Labs Ltd., Hyderabad | 2019
Out-of-stock
Issued on: May 13, 2019
Human Drug Form 483
FDA 483 Vimta Labs Ltd., Hyderabad | 2018
Out-of-stock
Issued on: Oct 26, 2018
Human Drug Form 483
FDA 483 Vimta Labs Ltd., Hyderabad | 2011
Out-of-stock
Issued on: Feb 18, 2011
Human Drug Form 483
FDA 483 Vimta Labs Ltd., Hyderabad | 2010
Out-of-stock
Issued on: Apr 22, 2010
Human Drug Form 483
FDA 483 Vimta Labs Ltd., Hyderabad | 2008
Out-of-stock
Issued on: Mar 5, 2008
Human Drug Form 483
FDA 483 Vimta Labs Ltd., Hyderabad | 2006
Out-of-stock
Issued on: Sep 15, 2006
Human Drug Form 483
FDA 483 Vimta Labs Ltd., Hyderabad | 2006
Out-of-stock
Issued on: Jun 16, 2006
Human Drug Form 483
FDA 483 Vimta Labs Ltd., Hyderabad | 2005
Out-of-stock
Issued on: Aug 11, 2005
Human Drug Form 483
FDA Investigators(15)
- Janete F. Guardia, FDA Investigator
- Zhou Chen, FDA Investigator
- Mark J. Seaton, FDA Investigator
- Kellia N. Hicks, FDA Investigator
- Jennifer C. Adams, FDA Investigator
- Sripal R. Mada, FDA Investigator
- Gajendiran Mahadevan, FDA Investigator
- Sony Mathews, FDA Investigator
- Barbara J. Rincon, FDA Investigator
- Kathryn A. Krentz, FDA Investigator
- David R. Heiar, FDA Investigator
- Andrea A. Branche, FDA Investigator
- Gerald N. McGirl, FDA Investigator
- Allen F. Hall, FDA Investigator
- Sriram Subramaniam, FDA Investigator