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FDA Inspection 1031100 — Horiba Instruments Incorporated

Horiba Instruments Incorporated — FEI 1827821

The FDA completed an inspection of Horiba Instruments Incorporated on October 31, 2017 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
October 31, 2017
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Canton, MI (United States)

Facility

Other inspections at this facility

  • 931697 (OAI Tue Jun 30 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 815527 (NAI Thu Jan 24 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 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