FDA Warning Letter — MEDICAMAT S.A.

Case 391311 — FEI 3002642065

The FDA took a Warning Letter action against MEDICAMAT S.A. on Apr 19, 2013 (Malakoff, France). The action was issued by CDRH and concerns devices products. This facility has 1 recent FDA inspection on record.

Action details

Facility
MEDICAMAT S.A.
Date
Apr 19, 2013
Fiscal Year
2013
Product Type
Devices
Center
CDRH
Location
Malakoff (France)

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