FDA Inspection 1226761 — Rex Implants

Rex Implants — FEI 3014174860

The FDA completed an inspection of Rex Implants on Dec 14, 2023 in Columbus, OH. 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
Dec 14, 2023
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
Columbus, OH (United States)

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