FDA Inspection 917051 — Endologix, Inc.

Endologix, Inc. — FEI 3008011247

The FDA completed an inspection of Endologix, Inc. on March 5, 2015 in Santa Rosa, 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
March 5, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Santa Rosa, CA (United States)