FDA Inspection 1264619 — ReliefBand Technologies

ReliefBand Technologies — FEI 3006614152

The FDA completed an inspection of ReliefBand Technologies on February 28, 2025 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
February 28, 2025
Fiscal Year
2025
Product Type
Devices
Project Area
Compliance: Devices
Location
Horsham, PA (United States)