FDA Inspection 742920 — Endologix, Inc.

Endologix, Inc. — FEI 3008011247

The FDA completed an inspection of Endologix, Inc. on September 1, 2011 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
September 1, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Santa Rosa, CA (United States)