FDA Warning Letter — Cardionics SA

Case 478690 — FEI 3003675391

The FDA took a Warning Letter action against Cardionics SA on October 21, 2015 (Sint-Jans-Molenbeek, Belgium). The action was issued by CDRH and concerns devices products. This facility has 1 recent FDA inspection on record.

Action Details

Facility
Cardionics SA
Date
October 21, 2015
Fiscal Year
2016
Product Type
Devices
Center
CDRH
Location
Sint-Jans-Molenbeek (Belgium)