FDA Investigator: Jean M. Kelahan

- Jean M. Kelahan first started conducting FDA inspections in 2000, with the last inspection in 2008. Over that time, Jean M. Kelahan has conducted 85 inspections at 76 companies across 75 sites.

Get Jean Kelahan's official FDA inspection documents. Gain valuable insights from their Form 483s and EIRs to ace your next inspection.

Documents

Upon purchase, you will receive an email with a link to immediately download the documents.

FDA 483 Ocean Medical Center IRB, Brick | 2007

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Jean M. Kelahan
Medical Devices & Rad Health Form 483

FDA 483 Novartis Pharmaceuticals Corp., East Hanover | 2007

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Jean M. Kelahan
Human Drug Form 483

FDA 483 Huntingdon Life Sciences, Inc., East Millstone | 2007

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Jean M. Kelahan
Human Drug Form 483

FDA 483 Monmouth Medical Center IRB, Long Branch | 2007

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Jean M. Kelahan
Biologic Form 483

FDA 483 Shelhigh, Inc., Union | 2006

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Jean M. Kelahan
Medical Devices & Rad Health Form 483

FDA 483 Peter M. Scholz, M.D., New Brunswick | 2006

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Jean M. Kelahan
Medical Devices & Rad Health Form 483

FDA 483 Organon, a part of Schering-Plough Corporation, Roseland | 2006

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Jean M. Kelahan
Human Drug Form 483

FDA 483 UMDNJ Institutional Review Board, New Brunswick Campus, New Brunswick | 2006

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Jean M. Kelahan
Human Drug Form 483

FDA 483 Sachdeo Rajesh C MD, New Brunswick | 2006

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Jean M. Kelahan
Human Drug Form 483

FDA 483 Bristol Myers Squibb Company, Pennington | 2005

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Jean M. Kelahan
Human Drug Form 483

FDA 483 UMDNJ - RWJ Univ. Orthopaedic Group, New Brunswick | 2005

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Jean M. Kelahan
Medical Devices & Rad Health Form 483

FDA 483 Shelhigh, Inc., Union | 2005

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Jean M. Kelahan
Medical Devices & Rad Health Form 483