FDA Documents of Lotus Laboratories Pvt. Ltd.
Lotus Laboratories Pvt. Ltd. is an organization that has been audited by the FDA 15 times between 2005 and 2023 across all 6 sites.
Documents
FDA 483 Lotus Laboratories Pvt. Ltd., Bangalore | 2010
Out-of-stock
Issued on: Nov 8, 2010
Human Drug Form 483
FDA 483 Lotus Laboratories Pvt. Ltd., Bangalore | 2010
Out-of-stock
Issued on: May 6, 2010
Human Drug Form 483
FDA 483 Lotus Laboratories Pvt. Ltd., Bangalore | 2009
Out-of-stock
Issued on: Apr 10, 2009
Human Drug Form 483
FDA 483 Lotus Laboratories Pvt. Ltd., Koramangala II Block, Bangalore | 2009
Out-of-stock
Issued on: Apr 3, 2009
Human Drug Form 483
FDA 483 Lotus Laboratories Pvt. Ltd., Bangalore | 2007
Out-of-stock
Issued on: Feb 23, 2007
Human Drug Form 483
FDA 483 Lotus Laboratories Pvt. Ltd., Bangalore | 2006
Out-of-stock
Issued on: Sep 1, 2006
Human Drug Form 483
FDA 483 Lotus Laboratories Pvt. Ltd., Bangalore | 2005
Out-of-stock
Issued on: Aug 25, 2005
Human Drug Form 483
FDA Investigators(16)
- Anna M. Brannen, FDA Investigator
- Courtney N. Long, FDA Investigator
- Dawn C. Olenjack, FDA Investigator
- Melkamu Getie Kebtie, FDA Investigator
- Gajendiran Mahadevan, FDA Investigator
- Getie Kebtie, Melkamu, FDA Investigator
- Nicola M. Fenty-Stewart, FDA Investigator
- Douglas Fiorentino, FDA Investigator
- Arindam Dasgupta, FDA Investigator
- Rochelle B. Young, FDA Investigator
- Minh D. Phan, FDA Investigator
- David R. Heiar, FDA Investigator
- Robert C. Steyert, FDA Investigator
- Gerald Mierle, FDA Investigator
- Linda R. Kuchenthal, FDA Investigator
- Sriram Subramaniam, FDA Investigator