FDA Inspection 1214366 — Kolmar Korea Co. Ltd. - Gwanjeong 2 Branch

Kolmar Korea Co. Ltd. - Gwanjeong 2 Branch — FEI 3011437246

The FDA completed an inspection of Kolmar Korea Co. Ltd. - Gwanjeong 2 Branch on July 21, 2023 in Sejong. 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 21, 2023
Fiscal Year
2023
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Sejong (Korea (the Republic of))