FDA Investigator: Shirley H. Isbill
- Shirley H. Isbill first started conducting FDA inspections in 2000, with the last inspection in 2005. Over that time, Shirley H. Isbill has conducted 24 inspections at 24 companies across 24 sites.
Get Shirley Isbill'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 Able Laboratories Inc., New Brunswick | 2005
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Shirley H. Isbill
Human Drug Form 483
FDA 483 Dr. Paul Devroey, Brussels | 2004
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Shirley H. Isbill
Human Drug Form 483
FDA 483 Dr. Robert H.G. Schwinger, Koln | 2004
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Shirley H. Isbill
Human Drug Form 483
FDA 483 Dr. Nicholas H. Brooks, Wythenshawe, Manchester | 2004
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Shirley H. Isbill
Human Drug Form 483
FDA 483 Kaladas, Jeffrey J., MD, South Bound Brook | 2004
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Shirley H. Isbill
Human Drug Form 483
FDA 483 Bachmann, Gloria A., MD, New Brunswick | 2004
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Shirley H. Isbill
Human Drug Form 483
FDA 483 International Pharmaceutical Research Center (IPRC), Amman | 2003
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Shirley H. Isbill
Human Drug Form 483
FDA 483 Marc Dubuc, M.D., Montreal | 2003
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Shirley H. Isbill
Medical Devices & Rad Health Form 483
FDA 483 Medtronic CryoCath LP, Kirkland | 2003
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Shirley H. Isbill
Medical Devices & Rad Health Form 483
FDA 483 Comprehensive Clinical Research, Berlin | 2001
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Shirley H. Isbill
Human Drug Form 483
FDA 483 Howard Yanofsky, M.D. #1, Montreal | 2000
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Shirley H. Isbill
Human Drug Form 483