FDA Inspection 932609 — Apixia Inc

Apixia Inc — FEI 3008361230

The FDA completed an inspection of Apixia Inc on June 11, 2015 in City Of Industry, 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
June 11, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
City Of Industry, CA (United States)