FDA Inspection 708074 — SUZUKEN CO., LTD. OGUCHI CENTER
The FDA completed an inspection of SUZUKEN CO., LTD. OGUCHI CENTER on December 15, 2010 in Niwa-Gun. 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
- December 15, 2010
- Fiscal Year
- 2011
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Niwa-Gun (Japan)