FDA Warning Letter — Vygon GmbH & Co. KG

Case 429171 — FEI 3002808464

The FDA took a Warning Letter action against Vygon GmbH & Co. KG on August 4, 2014 (Aachen, Germany). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Vygon GmbH & Co. KG
Date
August 4, 2014
Fiscal Year
2014
Product Type
Devices
Center
CDRH
Location
Aachen (Germany)