FDA Inspection 821068 — Bioplexus LLC

Bioplexus LLC — FEI 1000221490

The FDA completed an inspection of Bioplexus LLC on Mar 6, 2013 in Kingman, AZ. 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
Mar 6, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Kingman, AZ (United States)