FDA Warning Letter — Avertix Medical, Inc.

Case 711080 — FEI 3017374019

The FDA took a Warning Letter action against Avertix Medical, Inc. on September 3, 2025 (Eatontown, NJ). The action was issued by CDRH and concerns devices products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
Avertix Medical, Inc.
Date
September 3, 2025
Fiscal Year
2025
Product Type
Devices
Center
CDRH
Location
Eatontown, NJ (United States)