FDA Investigator: Michelle M. Noe Varga
- Michelle M. Noe Varga first started conducting FDA inspections in 2013, with the last inspection in 2022. Over that time, Michelle M. Noe Varga has conducted 40 inspections at 39 companies across 39 sites.
Get Michelle Noe Varga'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 Andrea L. D. Orsey, M.D., Hartford | 2015
Out-of-stock
Michelle M. Noe Varga
Human Drug Form 483
FDA 483 Kent County Memorial Hospital Institutional Review Board, Warwick | 2015
Out-of-stock
Michelle M. Noe Varga
Human Drug Form 483
FDA 483 Steven P. Treon, M.D., PhD, Boston | 2014
Out-of-stock
Michelle M. Noe Varga
Human Drug Form 483
FDA 483 Christopher H. Comey, MD, Springfield | 2014
Out-of-stock
Michelle M. Noe Varga
Medical Devices & Rad Health Form 483
FDA 483 Suvranu Ganguli, MD, Boston | 2014
Out-of-stock
Michelle M. Noe Varga
Medical Devices & Rad Health Form 483
Co-Investigators (11)
- Michelle J. Hines, FDA Investigator
- Noe Varga, Michelle M, FDA Investigator
- Joy P. Matthias, FDA Investigator
- Iram R. Hassan, FDA Investigator
- Ruth A. Williams, FDA Investigator
- Matthew C. Watson, FDA Investigator
- Karen M. Cooper, FDA Investigator
- Michelle M. Noe, FDA Investigator
- Kent A. Conforti, FDA Investigator
- Sripal R. Mada, FDA Investigator
- Elizabeth B. Griffin, FDA Investigator