FDA Warning Letter — Luminex Corporation

Case 60643 — FEI 3002524000

The FDA took a Warning Letter action against Luminex Corporation on May 14, 2009 (Austin, TX). The action was issued by CDRH and concerns devices products. This facility has 4 recent FDA inspections on record.

Action Details

Facility
Luminex Corporation
Date
May 14, 2009
Fiscal Year
2009
Product Type
Devices
Center
CDRH
Location
Austin, TX (United States)