FDA Warning Letter — Alber GmbH

Case 532755 — FEI 3004730072

The FDA took a Warning Letter action against Alber GmbH on September 15, 2017 (Albstadt, Germany). The action was issued by CDRH and concerns devices products. This facility has 4 recent FDA inspections on record.

Action Details

Facility
Alber GmbH
Date
September 15, 2017
Fiscal Year
2017
Product Type
Devices
Center
CDRH
Location
Albstadt (Germany)