FDA Investigator: Bo Chi

- Bo Chi first started conducting FDA inspections in 2007, with the last inspection in 2024. Over that time, Bo Chi has conducted 46 inspections at 39 companies across 41 sites.

Get Bo Chi'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 Vetter Pharma Fertigung GmbH & Co. KG, Langenargen | 2024

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Bo Chi
Human Drugs Form 483

FDA 483 Vetter Pharma Fertigung GmbH & Co. KG (Ravensburg Mooswiesen), Ravensburg | 2024

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Bo Chi
Human Drugs Form 483

FDA 483 Novartis d.o.o., Menges | 2023

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Bo Chi
Human Drugs Form 483

FDA 483 Wuxi Biologics Co Ltd, Wuxi | 2023

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Bo Chi
Human Drugs Form 483

FDA 483 Seibersdorf Labor GmbH, Seibersdorf | 2022

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Bo Chi
Human Drugs Form 483

FDA 483 Nang Kuang Pharmaceutical Co., Ltd., Tainan City | 2022

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Bo Chi
Human Drug Form 483

FDA 483 Takeda Pharmaceuticals U.S.A., Brooklyn Park | 2020

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Bo Chi
Human Drug Form 483

FDA 483 Merz Pharma GmbH & Co., KGaA, Dessau-Rosslau | 2019

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Bo Chi
Human Drug Form 483

FDA 483 Biogen Idec (Denmark) Manufacturing ApS, Hillerod | 2019

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Bo Chi
Human Drug Form 483

FDA 483 Patheon Biologics LLC, Saint Louis | 2018

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Bo Chi
Human Drug Form 483

FDA 483 Exelead, Inc., Indianapolis | 2018

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Bo Chi
Human Drug Form 483

FDA 483 Amgen, Inc., Thousand Oaks | 2018

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Bo Chi
Human Drug Form 483

FDA 483 Chugai Pharmaceutical Co., Ltd., Kita | 2017

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Bo Chi
Human Drug Form 483

FDA 483 Wuxi Apptec Biopharmaceuticals Co Ltd, Wuxi | 2017

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Bo Chi
Human Drug Form 483

FDA 483 Lonza Biologics Porrino, O Porrino (Casco Urbano) | 2016

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Bo Chi
Human Drug Form 483

FDA 483 Lonza Biologics Porrino, O Porrino (Casco Urbano) | 2016

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Bo Chi
Human Drug Form 483

FDA 483 Amgen, Inc., Thousand Oaks | 2016

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Bo Chi
Human Drug Form 483