FDA Investigator: Gajendiran Mahadevan
- Gajendiran Mahadevan first started conducting FDA inspections in 2016, with the last inspection in 2023. Over that time, Gajendiran Mahadevan has conducted 29 inspections at 28 companies across 28 sites.
Get Gajendiran Mahadevan's official FDA inspection documents. Gain valuable insights from their Form 483s and EIRs to ace your next inspection.
Documents
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FDA 483 Daicel Chiral Technologies (India) Private Limited, Shamirpet | 2023
Out-of-stock
Gajendiran Mahadevan
Human Drugs Form 483
FDA 483 SGS Cephac Europe, St Benoit Cedex | 2018
Out-of-stock
Gajendiran Mahadevan
Human Drug Form 483
FDA 483 Nuvisan GmbH, Neu-Ulm | 2018
Out-of-stock
Gajendiran Mahadevan
Human Drug Form 483
FDA 483 Vimta Labs Limited, Hyderabad | 2018
Out-of-stock
Gajendiran Mahadevan
Human Drug Form 483
FDA 483 Covance Laboratories, Ltd., Harrogate | 2017
Out-of-stock
Gajendiran Mahadevan
Human Drug Form 483
Co-Investigators (16)
- Arindam Dasgupta, FDA Investigator
- Lori Gioia, FDA Investigator
- Amanda Lewin, FDA Investigator
- Hasan A. Irier, FDA Investigator
- Li-Hong P. Yeh, FDA Investigator
- Li-Hong Yeh, FDA Investigator
- Melkamu Getie Kebtie, FDA Investigator
- Getie Kebtie, Melkamu, FDA Investigator
- Sripal R. Mada, FDA Investigator
- Mohsen Rajabi Abhari, FDA Investigator
- Rajabi Abhari, Mohsen, FDA Investigator
- Ruben C. Ayala, FDA Investigator
- Jennifer C. Adams, FDA Investigator
- Kara A. Scheibner, FDA Investigator
- Nicola M. Fenty-Stewart, FDA Investigator
- Daniel J. Roberts, FDA Investigator