FDA Warning Letter — Maquet Cardiopulmonary Gmbh

Case 438658 — FEI 3009507273

The FDA took a Warning Letter action against Maquet Cardiopulmonary Gmbh on December 4, 2014 (Rastatt, Germany). The action was issued by CDRH and concerns devices products. This facility has 2 recent FDA inspections on record.

Action Details

Facility
Maquet Cardiopulmonary Gmbh
Date
December 4, 2014
Fiscal Year
2015
Product Type
Devices
Center
CDRH
Location
Rastatt (Germany)