FDA Warning Letter — TYRX Inc.

Case 497549 — FEI 3005619263

The FDA took a Warning Letter action against TYRX Inc. on June 2, 2016 (Monmouth Junction, NJ). The action was issued by CDRH and concerns devices products. This facility has 4 recent FDA inspections on record.

Action Details

Facility
TYRX Inc.
Date
June 2, 2016
Fiscal Year
2016
Product Type
Devices
Center
CDRH
Location
Monmouth Junction, NJ (United States)