FDA Investigator: Viviana Matta

- Viviana Matta first started conducting FDA inspections in 2010, with the last inspection in 2022. Over that time, Viviana Matta has conducted 128 inspections at 104 companies across 116 sites.

Get Viviana Matta'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 Corixa Corporation, Marietta | 2022

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Viviana Matta
Biologic Form 483

FDA 483 KBI Biopharma, Inc., Durham | 2020

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Viviana Matta
Human Drug Form 483

FDA 483 Patheon Manufacturing Services LLC, Greenville | 2020

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Viviana Matta
Human Drug Form 483

FDA 483 Catalent Belgium SA, Brussels | 2019

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Viviana Matta
Human Drug Form 483

FDA 483 Biogen U.S. Corporation, Research Triangle Park | 2018

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Viviana Matta
Human Drug Form 483

FDA 483 Janssen Sciences Ireland UC, Ringaskiddy | 2017

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Viviana Matta
Human Drug Form 483

FDA 483 Biogen MA Inc., Research Triangle Park | 2016

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Viviana Matta
Human Drug Form 483

Co-Investigators (53)