FDA Inspection 731898 — Aegis Spine Inc

Aegis Spine Inc — FEI 3008111283

The FDA completed an inspection of Aegis Spine Inc on May 24, 2011 in Walnut, 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 24, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Walnut, CA (United States)