FDA Warning Letter — Alseal

Case 507073 — FEI 3010149375

The FDA took a Warning Letter action against Alseal on Nov 10, 2016 (Besancon, France). The action was issued by CDRH and concerns devices products. This facility has 1 recent FDA inspection on record.

Action details

Facility
Alseal
Date
Nov 10, 2016
Fiscal Year
2017
Product Type
Devices
Center
CDRH
Location
Besancon (France)

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