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FDA Warning Letter — Luminex Corporation

Case 606267 — FEI 3002524000

The FDA took a Warning Letter action against Luminex Corporation on Jun 26, 2020 (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
Jun 26, 2020
Fiscal Year
2020
Product Type
Devices
Center
CDRH
Location
Austin, TX (United States)

Facility

Recent inspections

Other compliance actions

FDA data resources

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