FDA Inspection 1066351 — SEASPINE ORTHOPEDICS CORPORATION

SEASPINE ORTHOPEDICS CORPORATION — FEI 3012120772

The FDA completed an inspection of SEASPINE ORTHOPEDICS CORPORATION on Aug 14, 2018 in Carlsbad, 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
Aug 14, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Carlsbad, CA (United States)