FDA Investigator: Monique C. Lo
- Monique C. Lo first started conducting FDA inspections in 2002, with the last inspection in 2005. Over that time, Monique C. Lo has conducted 48 inspections at 46 companies across 46 sites.
Get Monique Lo'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 Greenberg, Peter, Palo Alto | 2005
Out-of-stock
Monique C. Lo
Human Drug Form 483
FDA 483 Paul Harmatz, M.D., Oakland | 2005
Out-of-stock
Monique C. Lo
Human Drug Form 483
Co-Investigators (17)
- Darlene B. Almogela, FDA Investigator
- Ronald P. Boyce, FDA Investigator
- Carla C. Tuite, FDA Investigator
- Elizabeth B. Griffin, FDA Investigator
- Paraluman S. Leonin, FDA Investigator
- Richard H. Penta, FDA Investigator
- Louis Christy, FDA Investigator
- Andrew M. Barlow, FDA Investigator
- Robert M. O Brien, FDA Investigator
- O Brien, Robert M, FDA Investigator
- Prabhu P. Raju, FDA Investigator
- David P. Vanhouten, FDA Investigator
- Paul P. Geraci, FDA Investigator
- Karen E. McNabb-Noon, FDA Investigator
- Aldo J. Quintana, FDA Investigator
- Ellen P. Madigan, FDA Investigator
- Jason A. Rossi, FDA Investigator