FDA Inspection 1010585 — AEGIS Spine, Inc.

AEGIS Spine, Inc. — FEI 3009790163

The FDA completed an inspection of AEGIS Spine, Inc. on May 9, 2017 in Englewood, CO. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
May 9, 2017
Fiscal Year
2017
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Englewood, CO (United States)