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FDA Inspection 931697 — Horiba Instruments Incorporated

Horiba Instruments Incorporated — FEI 1827821

The FDA completed an inspection of Horiba Instruments Incorporated on June 30, 2015 in Canton, MI. 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
June 30, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Canton, MI (United States)

Facility

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  • 782820 (NAI Fri Mar 09 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 706493 (NAI Fri Jan 28 2011 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 627000 (NAI Fri Jan 15 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources