FDA Warning Letter — Alseal

Case 507073 — FEI 3010149375

The FDA took a Warning Letter action against Alseal on November 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
November 10, 2016
Fiscal Year
2017
Product Type
Devices
Center
CDRH
Location
Besancon (France)