FDA Warning Letter — Simpro

Case 506504 — FEI 3004485927

The FDA took a Warning Letter action against Simpro on August 17, 2016 (Irving, TX). The action was issued by CDRH and concerns devices products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
Simpro
Date
August 17, 2016
Fiscal Year
2016
Product Type
Devices
Center
CDRH
Location
Irving, TX (United States)