Mesa Laboratories Bozeman Manufacturing Facility

FDA Regulatory Profile

Mesa Laboratories Bozeman Manufacturing Facility appears in FDA public data with 2 recalls, 0 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-1274-2018, Class II) was initiated on February 12, 2018.

Summary

Total Recalls
2
510(k) Clearances
0
Inspections
0
Compliance Actions
0

Recent Recalls

NumberClassProductDate
Z-1274-2018Class IISporAmpule Biological Indicator Catalog Number SPS5-100February 12, 2018
Z-1273-2018Class IIProSpore Biological Indicator Part Numbers: PS-6-50, PS-5-50, PS-4-10, PS-4-50, 3471February 12, 2018