FDA Warning Letter — MEDINVENTS NV

Case 396903 — FEI 3007513241

The FDA took a Warning Letter action against MEDINVENTS NV on Jun 6, 2013 (Hasselt, Belgium). The action was issued by CDRH and concerns devices products. This facility has 1 recent FDA inspection on record.

Action Details

Facility
MEDINVENTS NV
Date
Jun 6, 2013
Fiscal Year
2013
Product Type
Devices
Center
CDRH
Location
Hasselt (Belgium)

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