FDA Inspection 1247509 — Beckman Coulter, Inc.

Beckman Coulter, Inc. — FEI 2122870

The FDA completed an inspection of Beckman Coulter, Inc. on January 17, 2025 in Chaska, MN. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
January 17, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Chaska, MN (United States)

Additional Details

Sponsor, Contract Research Organization