Home / Compliance actions / 194932

FDA Warning Letter — Beckman Coulter Inc.

Case 194932 — FEI 2050012

The FDA took a Warning Letter action against Beckman Coulter Inc. on August 1, 2011 (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
August 1, 2011
Fiscal Year
2011
Product Type
Devices
Center
CDRH
Location
Brea, CA (United States)

Facility

Recent inspections

  • 1149891 (NAI Thu Aug 05 2021 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1111029 (NAI Wed Oct 30 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 791139 (NAI Mon Jul 16 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 725062 (OAI Thu May 12 2011 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 710437 (VAI Tue Feb 08 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

Other compliance actions

FDA data resources