FDA Inspection 964419 — BioFire Diagnostics, LLC

BioFire Diagnostics, LLC — FEI 3002773840

The FDA completed an inspection of BioFire Diagnostics, LLC on March 18, 2016 in Salt Lake City, UT. 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
March 18, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Salt Lake City, UT (United States)