FDA Inspection 971813 — Nihon Kohden Tomioka Corporation
The FDA completed an inspection of Nihon Kohden Tomioka Corporation on Mar 25, 2016 in Tomioka. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.
Inspection details
- Classification
- No Action Indicated (NAI)
- End Date
- Mar 25, 2016
- Fiscal Year
- 2016
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Tomioka (Japan)