FDA Investigator: Paul C. Mouris

- Paul C. Mouris first started conducting FDA inspections in 2004, with the last inspection in 2023. Over that time, Paul C. Mouris has conducted 123 inspections at 81 companies across 86 sites.

Get Paul Mouris'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 Greenbrier International, Inc, Chesapeake | 2019

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Paul C. Mouris
Human Drug Form 483

FDA 483 Cipla Limited, Pithampur, District Dhar | 2018

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Paul C. Mouris
Human Drug Form 483

FDA 483 Silarx Pharmaceutical, Inc., Carmel | 2013

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Paul C. Mouris
Human Drug Form 483

FDA 483 Fougera Pharmaceuticals, Inc., Melville | 2013

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Paul C. Mouris
Human Drug Form 483

FDA 483 Ultra Seal Corporation, New Paltz | 2013

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Paul C. Mouris
Human Drug Form 483

FDA 483 Corden Pharma Latina S.p.A., Sermoneta | 2013

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Paul C. Mouris
Human Drug Form 483

FDA 483 Corden Pharma Latina S.p.A., Sermoneta | 2013

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Paul C. Mouris
Human Drug Form 483

FDA 483 Pfizer Inc, Rouses Point | 2013

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Paul C. Mouris
Human Drug Form 483

FDA 483 Barr Laboratories, Inc. (subsidiary of Teva Pharmaceuticals), Pomona | 2013

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Paul C. Mouris
Human Drug Form 483

FDA 483 Regeneron Pharmaceuticals Inc, Tarrytown | 2013

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Paul C. Mouris
Human Drug Form 483

FDA 483 Velocity Pharma LLC, Farmingdale | 2013

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Paul C. Mouris
Human Drug Form 483

FDA 483 Novartis Pharmaceuticals Corp., Suffern | 2012

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Paul C. Mouris
Human Drug Form 483

Co-Investigators (44)