FDA Inspection 1064567 — Epix Orthopaedics

Epix Orthopaedics — FEI 3014545286

The FDA completed an inspection of Epix Orthopaedics on Aug 7, 2018 in Morgan Hill, 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 7, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Morgan Hill, CA (United States)