FDA Inspection 1340080 — Rex Implants

Rex Implants — FEI 3014174860

The FDA completed an inspection of Rex Implants on Oct 1, 2026 in Columbus, OH. 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
Oct 1, 2026
Fiscal Year
2027
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.