FDA Inspection 813482 — Anodyne Therapy, LLC

Anodyne Therapy, LLC — FEI 1000113231

The FDA completed an inspection of Anodyne Therapy, LLC on January 9, 2013 in Oldsmar, 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
January 9, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Oldsmar, FL (United States)