FDA Inspection 991209 — SpineNet LLC.

SpineNet LLC. — FEI 3006755626

The FDA completed an inspection of SpineNet LLC. on October 4, 2016 in Maitland, FL. 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
Postmarket Assurance: Devices
Location
Maitland, FL (United States)