FDA Investigator: Zhou Chen

- Zhou Chen first started conducting FDA inspections in 2015, with the last inspection in 2024. Over that time, Zhou Chen has conducted 35 inspections at 29 companies across 30 sites.

Get Zhou Chen'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 Joinn Laboratories Co. Ltd., Beijing | 2024

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Zhou Chen
Human Drugs Form 483

FDA 483 Suzhou Xishan Zhongke Drug R&D, Co. Ltd., Suzhou | 2024

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Zhou Chen
Human Drugs Form 483

FDA 483 Beijing Union-Genius Pharmaceutical Technology Development Co., Ltd., Beijing | 2024

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Zhou Chen
Human Drugs Form 483

FDA 483 Level Biotechnology Inc, New Taipei City | 2024

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Zhou Chen
Human Drugs Form 483

FDA 483 U.S. Army Medical Research Institute of Infectious Diseases, Fort Detrick | 2020

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Zhou Chen
Human Drug Form 483

FDA 483 Vimta Labs Ltd., Hyderabad | 2019

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Zhou Chen
Human Drug Form 483

FDA 483 Lovelace Biomedical Research Institute, Albuquerque | 2019

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Zhou Chen
Human Drug Form 483

FDA 483 Pharmaron, Beijing | 2019

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Zhou Chen
Human Drug Form 483

FDA 483 Level Biotechnology Inc, Tiapei | 2019

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Zhou Chen
Human Drug Form 483

FDA 483 JOINN Laboratories (Suzhou), Taicang | 2019

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Zhou Chen
Human Drug Form 483

FDA 483 Wuxi Apptec Suzhou Co.,Ltd, Suzhou | 2019

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Zhou Chen
Human Drug Form 483

FDA 483 Covance Laboratories, Inc., Madison | 2018

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Zhou Chen
Human Drug Form 483

FDA 483 Charles River Laboratories Preclinical Services, Reno | 2018

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Zhou Chen
Human Drug Form 483

FDA 483 National Shanghai Center for New Drug Safety Evaluation Ctr, Shanghai | 2018

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Zhou Chen
Human Drug Form 483

FDA 483 Yunnan Institute of Medicine, Kunming | 2018

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Zhou Chen
Human Drug Form 483