FDA Inspection 1028265 — Kolmar Korea Co. Ltd.

Kolmar Korea Co. Ltd. — FEI 3004033751

The FDA completed an inspection of Kolmar Korea Co. Ltd. on September 28, 2017 in Sejong. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Drugs.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
September 28, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Sejong (Korea (the Republic of))