FDA Investigator: Junho Pak

- Junho Pak first started conducting FDA inspections in 2010, with the last inspection in 2024. Over that time, Junho Pak has conducted 111 inspections at 106 companies across 108 sites.

Get Junho Pak'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 Qilu Pharmaceutical Co., Ltd. (Dongjia Site), Jinan | 2024

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Junho Pak
Human Drugs Form 483

FDA 483 Alembic Pharmaceuticals Limited, Panelav | 2024

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Junho Pak
Human Drugs Form 483

FDA 483 Sun Pharmaceutical Medicare Limited, Halol | 2024

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Junho Pak
Human Drugs Form 483

FDA 483 BioAnalysis, LLC, Philadelphia | 2024

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Junho Pak
Human Drugs Form 483

FDA 483 Fidelio Healthcare Limburg GmbH, Limburg | 2023

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Junho Pak
Human Drugs Form 483

FDA 483 Eurofins PROXY Laboratories B.V., Leiden | 2023

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Junho Pak
Human Drugs Form 483

FDA 483 Hybio Pharmaceutical Co., Ltd. (Pingshan Factory), Shenzhen | 2023

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Junho Pak
Human Drugs Form 483

FDA 483 Tianjin Hope Technology Testing Co., Ltd., Tianjin | 2023

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Junho Pak
Human Drugs Form 483

FDA 483 OLIC (Thailand) Limited, Bang Pa-In | 2023

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Junho Pak
Human Drugs Form 483

FDA 483 Shree Jaya Laboratories, Nalgonda | 2022

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Junho Pak
Human Drugs Form 483

Co-Investigators (50)