FDA Inspection 1085816 — Sakura Seiki Co., Ltd. Yawata Factory
The FDA completed an inspection of Sakura Seiki Co., Ltd. Yawata Factory on February 15, 2019 in Chikuma. 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
- February 15, 2019
- Fiscal Year
- 2019
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Chikuma (Japan)