FDA Warning Letter — Beckman Coulter, Inc.

Case 213253 — FEI 3000203293

The FDA took a Warning Letter action against Beckman Coulter, Inc. on November 1, 2011 (Miami, FL). The action was issued by CDRH and concerns devices products. This facility has 4 recent FDA inspections on record.

Action Details

Facility
Beckman Coulter, Inc.
Date
November 1, 2011
Fiscal Year
2012
Product Type
Devices
Center
CDRH
Location
Miami, FL (United States)