FDA Inspection 1256315 — Kolmar Korea Co., Ltd. Bucheon Factory
The FDA completed an inspection of Kolmar Korea Co., Ltd. Bucheon Factory on Dec 6, 2024 in Bucheon. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.
Inspection details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Dec 6, 2024
- Fiscal Year
- 2025
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Bucheon (Korea (the Republic of))