FDA Inspection 930474 — ELITechGroup, Inc.

ELITechGroup, Inc. — FEI 1717966

The FDA completed an inspection of ELITechGroup, Inc. on May 27, 2015 in Logan, UT. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 3 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
May 27, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Logan, UT (United States)

Citations

IDCFRDescription
317221 CFR 820.198(c)Investigation of device failures
369621 CFR 820.100(b)Documentation
73121 CFR 803.50(a)(1)Report of Death or Serious Injury