FDA Investigator: Murphy, M. P
- Murphy, M. P first started conducting FDA inspections in 2000, with the last inspection in 2019. Over that time, Murphy, M. P has conducted 405 inspections at 272 companies across 273 sites.
Get Murphy, M. P'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 EIR Boehringer Ingelheim Pharmaceuticals, Danbury | 2010
Available Now - $995
Murphy, M. P
Human Drug Form 483
483 Response Boehringer Ingelheim Pharmaceuticals | Sep 2010
Available Now - $299
Murphy, M. P
Human Drug Form 483
Co-Investigators (31)
- Mary P. Murphy, FDA Investigator
- M. P. Murphy, FDA Investigator
- Gerald T. O'Connor, FDA Investigator
- O'Connor, Gerald T, FDA Investigator
- Sheri L. Stephenson, FDA Investigator
- Gabriel E. Muniz, FDA Investigator
- Jamie S. Mathews, FDA Investigator
- Anthony N. Onianwa, FDA Investigator
- Michelle M. Noe, FDA Investigator
- George T. Allen, FDA Investigator
- Dawn M. Braswell, FDA Investigator
- Diane C. Thibodeau, FDA Investigator
- Janete F. Guardia, FDA Investigator
- Douglas Fiorentino, FDA Investigator
- Matthew C. Watson, FDA Investigator
- Amy C. Jordan, FDA Investigator
- Mark R. McClain, FDA Investigator
- Maya M. Davis, FDA Investigator
- Karen E. McNabb-Noon, FDA Investigator
- Darin S. Wiegers, FDA Investigator
- Sriram Subramaniam, FDA Investigator
- Paula M. Laplant, FDA Investigator
- Gary J. Hagan, FDA Investigator
- Michael J. Leal, FDA Investigator
- Todd D. Alspach, FDA Investigator
- Sherry M. Nisson, FDA Investigator
- Jay M. Patria, FDA Investigator
- Stephen Souza, FDA Investigator
- Anthony C. Warchut, FDA Investigator
- John J. Thibodeau, FDA Investigator
- Ellen P. Madigan, FDA Investigator