FDA Inspection 971081 — Endologix LLC

Endologix LLC — FEI 3011063223

The FDA completed an inspection of Endologix LLC on May 20, 2016 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
May 20, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Irvine, CA (United States)