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FDA Inspection 1035440 — Mesa Laboratories, Inc., Bozeman Manufacturing Facility

Mesa Laboratories, Inc., Bozeman Manufacturing Facility — FEI 3013667284

The FDA completed an inspection of Mesa Laboratories, Inc., Bozeman Manufacturing Facility on December 7, 2016 in Bozeman, MT. 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
December 7, 2016
Fiscal Year
2017
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Bozeman, MT (United States)

Facility

Other inspections at this facility

  • 1095806 (NAI Fri Jun 14 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 926278 (NAI Thu May 14 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 799635 (NAI Thu Sep 20 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 782611 (VAI Fri May 11 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 735987 (NAI Wed Jul 13 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources