FDA Warning Letter — Luminex Corporation

Case 430264 — FEI 3006028115

The FDA took a Warning Letter action against Luminex Corporation on January 21, 2015 (Northbrook, IL). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Luminex Corporation
Date
January 21, 2015
Fiscal Year
2015
Product Type
Devices
Center
CDRH
Location
Northbrook, IL (United States)