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FDA Inspection 725062 — Beckman Coulter Inc.

Beckman Coulter Inc. — FEI 2050012

The FDA completed an inspection of Beckman Coulter Inc. on May 12, 2011 in Brea, CA. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
May 12, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Brea, CA (United States)

Facility

Other inspections at this facility

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  • 1111029 (NAI Wed Oct 30 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 791139 (NAI Mon Jul 16 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 710437 (VAI Tue Feb 08 2011 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 643446 (NAI Tue Dec 08 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources