FDA Warning Letter — ARCO2014

Case 500510 — FEI 3011496736

The FDA took a Warning Letter action against ARCO2014 on August 3, 2016 (Travagliato, Italy). The action was issued by CDRH and concerns devices products. This facility has 1 recent FDA inspection on record.

Action Details

Facility
ARCO2014
Date
August 3, 2016
Fiscal Year
2016
Product Type
Devices
Center
CDRH
Location
Travagliato (Italy)