FDA Inspection 1286314 — Orthorebirth Co Ltd

Orthorebirth Co Ltd — FEI 3011415547

The FDA completed an inspection of Orthorebirth Co Ltd on Sep 22, 2025 in Yokohama. The inspection was classified OAI (Official Action Indicated — regulatory and/or administrative actions are recommended). Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI)
End Date
Sep 22, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
Yokohama (Japan)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.