FDA Inspection 1224836 — Beckman Coulter, Inc.

Beckman Coulter, Inc. — FEI 2122870

The FDA completed an inspection of Beckman Coulter, Inc. on Dec 11, 2023 in Chaska, MN. The inspection was classified OAI (Official Action Indicated — regulatory and/or administrative actions are recommended). Product area: Devices.

Inspection Details

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

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