FDA Warning Letter — Beckman Coulter Inc.

Case 194932 — FEI 2050012

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

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.