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