FDA Investigator: Zhong Li

- Zhong Li first started conducting FDA inspections in 2015, with the last inspection in 2024. Over that time, Zhong Li has conducted 42 inspections at 38 companies across 41 sites.

Get Zhong Li'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 Patheon Manufacturing Services LLC, Greenville | 2024

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Zhong Li
Human Drugs Form 483

FDA 483 Akeso Biopharma, Co., Ltd., Zhongshan | 2023

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Zhong Li
Human Drugs Form 483

FDA 483 BeiGene (Suzhou) Co., Ltd., Suzhou | 2023

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Zhong Li
Human Drugs Form 483

FDA 483 Boehringer Ingelheim Biopharmaceuticals (China) Ltd., Shanghai | 2023

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Zhong Li
Human Drugs Form 483

FDA 483 Hugel Inc., Chuncheon | 2023

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Zhong Li
Human Drugs Form 483

FDA 483 Janssen Vaccines Corp., Incheon | 2023

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Zhong Li
Human Drugs Form 483

FDA 483 Alexion Pharma International Operations Unlimited Co., Dublin 15 | 2023

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Zhong Li
Human Drugs Form 483

FDA 483 Patheon Italia S.p.A., Monza | 2022

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Zhong Li
Human Drugs Form 483

FDA 483 Sharp Packaging Services, LLC, Allentown | 2022

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Zhong Li
Human Drugs Form 483

FDA 483 Biocon Biologics Limited, Bengaluru | 2022

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Zhong Li
Human Drug Form 483

FDA 483 Biocon Biologics Limited, Bengaluru | 2022

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Zhong Li
Human Drugs Form 483

FDA 483 Merck Serono SA Aubonne, Aubonne | 2022

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Zhong Li
Human Drugs Form 483

FDA 483 Curia New Mexico, LLC, Albuquerque | 2022

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Zhong Li
Human Drug Form 483

FDA 483 Curia New Mexico, LLC, Albuquerque | 2022

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Zhong Li
Human Drugs Form 483

FDA 483 Kyowa Hakko Kirin Co., Ltd., Takasaki | 2021

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Zhong Li
Human Drug Form 483

FDA 483 Chugai Pharma Manufacturing Co. Ltd. (CPMC), Kita | 2021

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Zhong Li
Human Drug Form 483

FDA 483 Macrogenics, Inc, Rockville | 2021

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Zhong Li
Human Drug Form 483