FDA Inspection 1286314 — Orthorebirth Co Ltd
The FDA completed an inspection of Orthorebirth Co Ltd on September 22, 2025 in Yokohama. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- September 22, 2025
- Fiscal Year
- 2025
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Yokohama (Japan)