FDA Inspection 797087 — Endologix, Inc.

Endologix, Inc. — FEI 3008011247

The FDA completed an inspection of Endologix, Inc. on August 31, 2012 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
August 31, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Santa Rosa, CA (United States)

Additional Details

Sponsor, Contract Research Organization