FDA Warning Letter — Beckman Coulter, Inc.

Case 678042 — FEI 2122870

The FDA took a Warning Letter action against Beckman Coulter, Inc. on March 15, 2024 (Chaska, MN). 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
March 15, 2024
Fiscal Year
2024
Product Type
Devices
Center
CDRH
Location
Chaska, MN (United States)