FDA Inspection 1247509 — Beckman Coulter, Inc.

Beckman Coulter, Inc. — FEI 2122870

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

Inspection Details

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

Additional Details

Sponsor, Contract Research Organization

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