FDA Inspection 1087335 — Kolmar Korea Co., Ltd. Bucheon Factory
The FDA completed an inspection of Kolmar Korea Co., Ltd. Bucheon Factory on March 22, 2019 in Bucheon. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- March 22, 2019
- Fiscal Year
- 2019
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Bucheon (Korea (the Republic of))