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FDA Inspection 985577 — Hanlim Pharm Co. Ltd.

Hanlim Pharm Co. Ltd. — FEI 3004886113

The FDA completed an inspection of Hanlim Pharm Co. Ltd. on July 19, 2016 in Yongin. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
July 19, 2016
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Yongin (Korea (the Republic of))

Facility

Other inspections at this facility

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  • 1316122 (NAI Fri Apr 10 2026 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1171848 (VAI Tue May 31 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1039954 (OAI Tue Feb 06 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 879041 (VAI Fri Apr 18 2014 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources