FDA Inspection 1339850 — 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 Sep 23, 2026 in Bozeman, MT. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Sep 23, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Compliance: Devices
Location
Bozeman, MT (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.