FDA Investigator: Sharmila Shrestha
- Sharmila Shrestha first started conducting FDA inspections in 2018, with the last inspection in 2024. Over that time, Sharmila Shrestha has conducted 7 inspections at 7 companies across 7 sites.
Get Sharmila Shrestha'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 Lentigen Technology Inc, Gaithersburg | 2024
Out-of-stock
Sharmila Shrestha
Biologics Form 483
FDA 483 Resilience US, Inc., Durham | 2024
Out-of-stock
Sharmila Shrestha
Biologics Form 483
FDA 483 Micro Typing Systems, Inc., Pompano Beach | 2019
Out-of-stock
Sharmila Shrestha
Biologic Form 483
FDA 483 Medion Grifols Diagnostics AG, Dudingen | 2018
Out-of-stock
Sharmila Shrestha
Biologic Form 483
Co-Investigators (12)
- Prajakta A. Varadkar, FDA Investigator
- Christine Harman, FDA Investigator
- Alifiya H. Ghadiali, FDA Investigator
- Alan G. Baer,
- Laura K. Demaster,
- Y N. Nguyen,
- Anna R. Kwilas, FDA Investigator
- Jie He, FDA Investigator
- Priscilla M. Pastrana, FDA Investigator
- Susan M. Jackson, FDA Investigator
- Meihong Liu, FDA Investigator
- Gene D. Arcy, FDA Investigator