FDA Inspection 848046 — Beckman Coulter, Inc.

Beckman Coulter, Inc. — FEI 3000203293

The FDA completed an inspection of Beckman Coulter, Inc. on September 11, 2013 in Miami, FL. 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
September 11, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Miami, FL (United States)