FDA Inspection 781880 — OrthoDynamix, LLC

OrthoDynamix, LLC — FEI 3007270492

The FDA completed an inspection of OrthoDynamix, LLC on Apr 27, 2012 in Jacksonville, FL. 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
Apr 27, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Jacksonville, FL (United States)