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FDA Inspection 706493 — Horiba Instruments Incorporated

Horiba Instruments Incorporated — FEI 1827821

The FDA completed an inspection of Horiba Instruments Incorporated on January 28, 2011 in Canton, MI. 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
January 28, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: 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))
  • 627000 (NAI Fri Jan 15 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources