FDA Warning Letter — Cardionics SA

Case 478690 — FEI 3003675391

The FDA took a Warning Letter action against Cardionics SA on Oct 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
Oct 21, 2015
Fiscal Year
2016
Product Type
Devices
Center
CDRH
Location
Sint-Jans-Molenbeek (Belgium)

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