FDA Inspection 1035440 - Mesa Laboratories, Inc., Bozeman Manufacturing Facility - December 07, 2016

FDA Inspection 1035440 for Mesa Laboratories, Inc., Bozeman Manufacturing Facility on December 07, 2016. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1035440 for Mesa Laboratories, Inc., Bozeman Manufacturing Facility on December 07, 2016. Classification: Voluntary Action Indicated (VAI).

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Record Information

Company

Mesa Laboratories, Inc., Bozeman Manufacturing Facility

Inspection Date

December 7, 2016

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fd9ec0e1-8561-4885-a8b1-f510470e5f76

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