FDA Investigator: Mike M. Rashti
- Mike M. Rashti first started conducting FDA inspections in 2000, with the last inspection in 2011. Over that time, Mike M. Rashti has conducted 208 inspections at 157 companies across 148 sites.
Get Mike Rashti'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 Medtronic Bakken Research Center B.V., Maastricht | 2011
Out-of-stock
Mike M. Rashti
Medical Devices & Rad Health Form 483
FDA 483 Dr. Bruno Farah, Toulouse | 2011
Out-of-stock
Mike M. Rashti
Medical Devices & Rad Health Form 483
FDA 483 Gynecologic Oncology Group, Philadelphia | 2011
Out-of-stock
Mike M. Rashti
Human Drug Form 483
FDA 483 Chatwani, Ashwin M.D., Philadelphia | 2011
Out-of-stock
Mike M. Rashti
Medical Devices & Rad Health Form 483
Co-Investigators (10)
- Marcia Gelber, FDA Investigator
- Kendra A. Biddick, FDA Investigator
- Matthew R. Noonan, FDA Investigator
- Kendra L. Brooks, FDA Investigator
- Brian D. Young, FDA Investigator
- Hala L. Selby, FDA Investigator
- Linda M. Hoover, FDA Investigator
- Robert B. Shibuya, FDA Investigator
- Mark J. Seaton, FDA Investigator
- Anthony A. Charity, FDA Investigator