FDA Inspection 979897 — Ceterix Orthopaedics, Inc.

Ceterix Orthopaedics, Inc. — FEI 3009131204

The FDA completed an inspection of Ceterix Orthopaedics, Inc. on Aug 4, 2016 in Fremont, 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 4, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Fremont, CA (United States)