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FDA Inspection 782820 — Horiba Instruments Incorporated

Horiba Instruments Incorporated — FEI 1827821

The FDA completed an inspection of Horiba Instruments Incorporated on March 9, 2012 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
March 9, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Canton, MI (United States)

Facility

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  • 706493 (NAI Fri Jan 28 2011 00:00:00 GMT+0000 (Coordinated Universal Time))
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FDA data resources