FDA Inspection 1256315 — Kolmar Korea Co., Ltd. Bucheon Factory
The FDA completed an inspection of Kolmar Korea Co., Ltd. Bucheon Factory on December 6, 2024 in Bucheon. 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
- December 6, 2024
- Fiscal Year
- 2025
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Bucheon (Korea (the Republic of))