FDA Inspection 1226761 — Rex Implants

Rex Implants — FEI 3014174860

The FDA completed an inspection of Rex Implants on December 14, 2023 in Columbus, OH. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
December 14, 2023
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
Columbus, OH (United States)