FDA Warning Letter — LivaNova Deutschland GmbH

Case 484629 — FEI 3002808267

The FDA took a Warning Letter action against LivaNova Deutschland GmbH on December 29, 2015 (Munich, Germany). The action was issued by CDRH and concerns devices products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
LivaNova Deutschland GmbH
Date
December 29, 2015
Fiscal Year
2016
Product Type
Devices
Center
CDRH
Location
Munich (Germany)