FDA Inspection 783029 — Beckman Coulter, Inc.

Beckman Coulter, Inc. — FEI 2122870

The FDA completed an inspection of Beckman Coulter, Inc. on May 17, 2012 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
May 17, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Chaska, MN (United States)