FDA Inspection 1031095 — Dynatronics Corporation

Dynatronics Corporation — FEI 1719362

The FDA completed an inspection of Dynatronics Corporation on November 9, 2017 in Salt Lake City, UT. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
November 9, 2017
Fiscal Year
2018
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Salt Lake City, UT (United States)

Citations

IDCFRDescription
328221 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures
369621 CFR 820.100(b)Documentation