FDA Warning Letter — Ferrosan Medical Devices A/S

Case 474404 — FEI 3008478369

The FDA took a Warning Letter action against Ferrosan Medical Devices A/S on Sep 16, 2015 (Soborg, Denmark). The action was issued by CDRH and concerns devices products. This facility has 1 recent FDA inspection on record.

Action Details

Facility
Ferrosan Medical Devices A/S
Date
Sep 16, 2015
Fiscal Year
2015
Product Type
Devices
Center
CDRH
Location
Soborg (Denmark)

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