FDA Inspection 950683 — Orthorebirth Co Ltd
The FDA completed an inspection of Orthorebirth Co Ltd on Nov 19, 2015 in Yokohama. 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
- Nov 19, 2015
- Fiscal Year
- 2016
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Yokohama (Japan)