FDA Inspection 778025 — Biogennix LLC

Biogennix LLC — FEI 3008773560

The FDA completed an inspection of Biogennix LLC on Apr 18, 2012 in Irvine, CA. 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
Apr 18, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Irvine, CA (United States)