FDA Investigator: Kerun Hardeo
- Kerun Hardeo first started conducting FDA inspections in 2022, with the last inspection in 2024. Over that time, Kerun Hardeo has conducted 34 inspections at 34 companies across 33 sites.
Get Kerun Hardeo'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 J. John Mann, M.D, New York | December 2023
Available Now - $199
Kerun Hardeo
Human Drugs Form 483
FDA 483 Applied Therapeutics, Inc., New York | 2024
Out-of-stock
Kerun Hardeo
Human Drugs Form 483
FDA 483 ICON Laboratory Services, Inc., Whitesboro | 2024
Out-of-stock
Kerun Hardeo
Human Drugs Form 483
FDA 483 Jack Michael Mann, M.D., Bayside | 2022
Out-of-stock
Kerun Hardeo
Human Drugs Form 483
FDA 483 Memorial Sloan-Kettering Cancer Center, New York | 2022
Out-of-stock
Kerun Hardeo
Biologic Form 483
FDA 483 Columbia University Medical Center IRB, New York | 2022
Out-of-stock
Kerun Hardeo
Biologic Form 483
FDA 483 NYC Health + Hospitals/Bellevue, New York | 2022
Out-of-stock
Kerun Hardeo
Biologic Form 483
FDA 483 CYN CHRISS IMPORTS CORP, New York | 2022
Out-of-stock
Kerun Hardeo
Foods & Cosmetic Form 483
Co-Investigators (13)
- Omadevi Somai, FDA Investigator
- Lucilla Facchin, FDA Investigator
- Nigel L. Hirth, FDA Investigator
- Benton M. Ketron, FDA Investigator
- Cheryl A. Grandinetti, FDA Investigator
- Yiying E. Chen, FDA Investigator
- Bernardica T. Sculac-Stern, FDA Investigator
- Iram R. Hassan, FDA Investigator
- Brandy D. Brown, FDA Investigator
- Byungja E. Marciante, FDA Investigator
- Jonathan D. Green, FDA Investigator
- Irina Gaberman, FDA Investigator
- Yuyan Liang, FDA Investigator