FDA Inspection 896405 — SeaSpine Inc

SeaSpine Inc — FEI 3003790069

The FDA completed an inspection of SeaSpine Inc on Sep 19, 2014 in Vista, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Sep 19, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Vista, CA (United States)