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FDA Inspection 782611 — 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 May 11, 2012 in Bozeman, MT. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
May 11, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: 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))
  • 1035440 (NAI Wed Dec 07 2016 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))
  • 735987 (NAI Wed Jul 13 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources