FDA Investigator: Kshitij A. Patkar
- Kshitij A. Patkar first started conducting FDA inspections in 2013, with the last inspection in 2024. Over that time, Kshitij A. Patkar has conducted 8 inspections at 8 companies across 8 sites.
Get Kshitij Patkar'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 Changzhou Yinsheng Pharmaceutical Co. Ltd., Changzhou | 2024
Out-of-stock
Kshitij A. Patkar
Human Drugs Form 483
FDA 483 Changzhou Sunlight Pharmaceutical Co., Ltd., Changzhou | 2024
Out-of-stock
Kshitij A. Patkar
Human Drugs Form 483
FDA 483 Synthon, s.r.o., Blansko | 2023
Out-of-stock
Kshitij A. Patkar
Human Drugs Form 483
FDA 483 Mylan Pharmaceuticals Inc, Morgantown | 2017
Out-of-stock
Kshitij A. Patkar
Human Drug Form 483
FDA 483 Sigma-Aldrich Mfg LLC, Saint Louis | 2017
Out-of-stock
Kshitij A. Patkar
Human Drug Form 483
FDA 483 Akorn, Inc., Decatur | 2013
Out-of-stock
Kshitij A. Patkar
Human Drug Form 483
Co-Investigators (13)
- Robin P. Mathew, FDA Investigator
- Jeffrey P. Raimondi, FDA Investigator
- Andrew J. Barrowcliff, FDA Investigator
- Jing Fang, FDA Investigator
- Nancy M. Espinal, FDA Investigator
- Sneha S. Patel, FDA Investigator
- Rebecca E. Dombrowski, FDA Investigator
- Rita K. Kabaso, FDA Investigator
- Michele Perry-Williams, FDA Investigator
- Frank Wackes, FDA Investigator
- Nicholas P. Diorio, FDA Investigator
- Joshua M. Adams, FDA Investigator
- Denise M. Digiulio, FDA Investigator