FDA Inspection 1224836 — Beckman Coulter, Inc.

Beckman Coulter, Inc. — FEI 2122870

The FDA completed an inspection of Beckman Coulter, Inc. on December 11, 2023 in Chaska, MN. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
December 11, 2023
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
Chaska, MN (United States)