FDA Inspection 791139 — Beckman Coulter Inc.

Beckman Coulter Inc. — FEI 2050012

The FDA completed an inspection of Beckman Coulter Inc. on July 16, 2012 in Brea, CA. 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
July 16, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Brea, CA (United States)