FDA Warning Letter — Rex Implants

Case 676429 — FEI 3014174860

The FDA took a Warning Letter action against Rex Implants on Mar 12, 2025 (Columbus, OH). The action was issued by CDRH and concerns devices products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
Rex Implants
Date
Mar 12, 2025
Fiscal Year
2025
Product Type
Devices
Center
CDRH
Location
Columbus, OH (United States)

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