FDA Inspection 739475 — Dynatronics Corporation

Dynatronics Corporation — FEI 1719362

The FDA completed an inspection of Dynatronics Corporation on August 11, 2011 in Salt Lake City, UT. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
August 11, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Salt Lake City, UT (United States)

Citations

IDCFRDescription
310421 CFR 820.30(j)Design history file
312721 CFR 820.80(e)Documentation