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•Huons Co., Ltd. - Jecheon Factory•November 21, 2025

FDA 483 - Huons Co., Ltd. - Jecheon Factory - November 21, 2025

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Record Details

Huon Co., Ltd., a sterile drug manufacturer in Jecheon, Korea, was cited for significant data integrity issues, inadequate investigations into product complaints and out-of-specification results, and critical deficiencies in aseptic processing and sterilization validation. These observations indicate a severe lack of control over manufacturing processes and quality systems. This could potentially impact the safety and efficacy of drug products intended for the U.S. market.

Company
Huons Co., Ltd. - Jecheon Factory
Inspection Date
November 21, 2025
Product Type
Drugs
Office
Office of Inspections and Investigations
People
  • Steven A. Brettler (Consumer Safety Officer)
  • Eileen A. Liu
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ID · a70cc7c8-2a25-41ff-a254-5653e3dfb70f

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