FDA Warning Letter — Maquet Cardiovascular, LLC

Case 125431 — FEI 2242352

The FDA took a Warning Letter action against Maquet Cardiovascular, LLC on August 11, 2010 (Wayne, NJ). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Maquet Cardiovascular, LLC
Date
August 11, 2010
Fiscal Year
2010
Product Type
Devices
Center
CDRH
Location
Wayne, NJ (United States)