FDA Inspection 643825 — Applied Spine Technologies

Applied Spine Technologies — FEI 3005258318

The FDA completed an inspection of Applied Spine Technologies on February 1, 2010 in Rocky Hill, CT. 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
February 1, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Rocky Hill, CT (United States)