FDA Inspection 990045 — Ortho Development Corporation

Ortho Development Corporation — FEI 1000143502

The FDA completed an inspection of Ortho Development Corporation on October 4, 2016 in Draper, UT. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
October 4, 2016
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Draper, UT (United States)