FDA Inspection 1121786 — ReliefBand Technologies

ReliefBand Technologies — FEI 3006614152

The FDA completed an inspection of ReliefBand Technologies on November 15, 2019 in Horsham, PA. 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
November 15, 2019
Fiscal Year
2020
Product Type
Devices
Project Area
Compliance: Devices
Location
Horsham, PA (United States)