FDA Inspection 1241642 — Denka Co. Ltd.
The FDA completed an inspection of Denka Co. Ltd. on May 23, 2024 in Gosen. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- May 23, 2024
- Fiscal Year
- 2024
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Gosen (Japan)