FDA Investigator: Robert M. O Brien
- Robert M. O Brien first started conducting FDA inspections in 2002, with the last inspection in 2005. Over that time, Robert M. O Brien has conducted 55 inspections at 54 companies across 54 sites.
Get Robert O Brien'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 Biogen Idec, Inc., Cambridge | 2004
Out-of-stock
Robert M. O Brien
Human Drug Form 483
FDA 483 Beth Israel Deaconess Medical Center IRB, Boston | 2004
Out-of-stock
Robert M. O Brien
Human Drug Form 483
FDA 483 Microbiology Research Associates, Inc., Acton | 2004
Out-of-stock
Robert M. O Brien
Human Drug Form 483
FDA 483 Monson Companies, Inc., Leominster | 2004
Out-of-stock
Robert M. O Brien
Human Drug Form 483
FDA 483 EMD Serono, Inc., Rockland | 2003
Out-of-stock
Robert M. O Brien
Human Drug Form 483
Co-Investigators (15)
- O Brien, Robert M, FDA Investigator
- Andrew M. Barlow, FDA Investigator
- Thomas J. Murphy, FDA Investigator
- Jason A. Rossi, FDA Investigator
- Richard H. Penta, FDA Investigator
- Amber G. Wardwell, FDA Investigator
- Monique C. Lo, FDA Investigator
- Joseph Foley, FDA Investigator
- Christopher M. Elliott, FDA Investigator
- Troy R. Petrillo, FDA Investigator
- David P. Vanhouten, FDA Investigator
- Thomas Cote, FDA Investigator
- Timothy M. Glod, FDA Investigator
- Aldo J. Quintana, FDA Investigator
- Christopher K. Vantwuyver, FDA Investigator