FDA Warning Letter — Beckman Coulter Inc.

Case 114828 — FEI 2050012

The FDA took a Warning Letter action against Beckman Coulter Inc. on June 21, 2010 (Brea, CA). The action was issued by CDRH and concerns devices products. This facility has 5 or more recent FDA inspections on record.

Action Details

Facility
Beckman Coulter Inc.
Date
June 21, 2010
Fiscal Year
2010
Product Type
Devices
Center
CDRH
Location
Brea, CA (United States)