FDA Inspection 1111029 — Beckman Coulter Inc.

Beckman Coulter Inc. — FEI 2050012

The FDA completed an inspection of Beckman Coulter Inc. on Oct 30, 2019 in Brea, CA. 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
Oct 30, 2019
Fiscal Year
2020
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Brea, CA (United States)

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