FDA Warning Letter — LivaNova Deutschland GmbH

Case 206153 — FEI 3002808267

The FDA took a Warning Letter action against LivaNova Deutschland GmbH on August 2, 2011 (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
August 2, 2011
Fiscal Year
2011
Product Type
Devices
Center
CDRH
Location
Munich (Germany)