FDA Investigator: Keith M. Reilly

- Keith M. Reilly first started conducting FDA inspections in 2000, with the last inspection in 2004. Over that time, Keith M. Reilly has conducted 75 inspections at 66 companies across 68 sites.

Get Keith Reilly'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 Jubilant Cadista Pharmaceuticals, Inc., Salisbury | 2004

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Keith M. Reilly
Human Drug Form 483

FDA 483 Aronson Medical Respiratory Services, Essex | 2004

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Keith M. Reilly
Human Drug Form 483

FDA 483 McNeil PPC Inc., Parsippany | 2003

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Keith M. Reilly
Human Drug Form 483

FDA 483 MPT Delivery Systems, Inc., Paterson | 2003

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Keith M. Reilly
Human Drug Form 483

FDA 483 Aphena Pharma Solutions, Whippany | 2003

Out-of-stock
Keith M. Reilly
Human Drug Form 483