FDA Inspection 777057 — Inogen, Inc

Inogen, Inc — FEI 3004672275

The FDA completed an inspection of Inogen, Inc on April 4, 2012 in Goleta, 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
April 4, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Goleta, CA (United States)