FDA Warning Letter — Unetixs Vascular, Inc.

Case 598016 — FEI 1222117

The FDA took a Warning Letter action against Unetixs Vascular, Inc. on February 4, 2020 (Warwick, RI). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Unetixs Vascular, Inc.
Date
February 4, 2020
Fiscal Year
2020
Product Type
Devices
Center
CDRH
Location
Warwick, RI (United States)