FDA Inspection 966015 — Sankei Co., Ltd.
The FDA completed an inspection of Sankei Co., Ltd. on Apr 7, 2016 in Ichihara. 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: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Apr 7, 2016
- Fiscal Year
- 2016
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Ichihara (Japan)