FDA Inspection 1151568 — TRUERELIEF

TRUERELIEF — FEI 3015550326

The FDA completed an inspection of TRUERELIEF on August 13, 2021 in Santa Monica, CA. 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
August 13, 2021
Fiscal Year
2021
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Santa Monica, CA (United States)