FDA Investigator: Geneve M. Maxwell
- Geneve M. Maxwell first started conducting FDA inspections in 2012, with the last inspection in 2015. Over that time, Geneve M. Maxwell has conducted 6 inspections at 6 companies across 6 sites.
Get Geneve Maxwell'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 Sigma-Tau Pharmasource, Inc., Indianapolis | 2015
Out-of-stock
Geneve M. Maxwell
Human Drug Form 483
FDA 483 Midwest Compliance Laboratories, LLC, Terre Haute | 2014
Out-of-stock
Geneve M. Maxwell
Human Drug Form 483
FDA 483 Pharmacia & Upjohn LLC, Kalamazoo | 2013
Out-of-stock
Geneve M. Maxwell
Animal Drugs & Feed Form 483
FDA 483 L. Perrigo Co., Allegan | 2012
Out-of-stock
Geneve M. Maxwell
Human Drug Form 483
Co-Investigators (15)
- Geneve M. Parks, FDA Investigator
- Theodore N. Sietsema, FDA Investigator
- Erin M. Miller, FDA Investigator
- Jeffrey D. Meng, FDA Investigator
- Michael G. Truchan, FDA Investigator
- Emily J. Orban, FDA Investigator
- Sarah M. Meng, FDA Investigator
- Sarah M. Napier, FDA Investigator
- Robert M. Barbosa, FDA Investigator
- Michele L. Forster, FDA Investigator
- Philip A. Klimkewicz, FDA Investigator
- Rebecca E. Dombrowski, FDA Investigator
- Martha Sullivan Myrick, FDA Investigator
- Cheryl M. Monroe, FDA Investigator
- Sullivan Myrick, Martha, FDA Investigator