FDA Investigator: Rebecca E. Dombrowski

- Rebecca E. Dombrowski first started conducting FDA inspections in 2003, with the last inspection in 2019. Over that time, Rebecca E. Dombrowski has conducted 131 inspections at 88 companies across 91 sites.

Get Rebecca Dombrowski'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 Deva Holding AS - Cerkezkoy Subesi, Cerkezkoy | 2019

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Rebecca E. Dombrowski
Human Drug Form 483

FDA 483 Cipla Limited, Vasco Da Gama | 2018

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Rebecca E. Dombrowski
Human Drug Form 483

FDA 483 Catalent Pharma Solutions Limited, Swindon | 2018

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Rebecca E. Dombrowski
Human Drug Form 483

FDA 483 Mylan Pharmaceuticals Inc, Morgantown | 2017

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Rebecca E. Dombrowski
Human Drug Form 483

FDA 483 Par Sterile Products LLC, Rochester | 2016

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Rebecca E. Dombrowski
Human Drug Form 483

FDA 483 Cenexi, Fontenay Sous Bois | 2016

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Rebecca E. Dombrowski
Human Drug Form 483

FDA 483 F. Hoffmann-LaRoche Ltd., Basel | 2014

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Rebecca E. Dombrowski
Human Drug Form 483

FDA 483 American Pharmaceutical Ingredients LLC, Waterford | 2014

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Rebecca E. Dombrowski
Human Drug Form 483

FDA 483 Division of Nuclear Medicine PET Radiopharmaceutical Prd., Ann Arbor | 2014

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Rebecca E. Dombrowski
Human Drug Form 483

FDA 483 Spectron MRC, LLC, South Bend | 2013

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Rebecca E. Dombrowski
Human Drug Form 483

FDA 483 Children's Hospital of Michigan, PET Site, Detroit | 2013

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Rebecca E. Dombrowski
Human Drug Form 483

FDA 483 Bristol-Myers Squibb Company, Inc., Mount Vernon | 2013

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Rebecca E. Dombrowski
Human Drug Form 483

FDA 483 Praxair Inc., River Rouge | 2013

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Rebecca E. Dombrowski
Human Drug Form 483

Co-Investigators (73)