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FDA Inspection 635346 — Biomerieux Inc

Biomerieux Inc — FEI 1950204

The FDA completed an inspection of Biomerieux Inc on December 11, 2009 in Hazelwood, MO. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
December 11, 2009
Fiscal Year
2010
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Hazelwood, MO (United States)

Facility

Other inspections at this facility

  • 1100977 (VAI Tue Aug 20 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1000732 (VAI Wed Jan 25 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 929513 (VAI Tue Jun 09 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 891090 (OAI Wed Jul 30 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 817590 (VAI Tue Feb 05 2013 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources