FDA Inspection 1056975 — WalkMed Technologies, LLC

WalkMed Technologies, LLC — FEI 3000204189

The FDA completed an inspection of WalkMed Technologies, LLC on June 26, 2018 in Aurora, CO. 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
June 26, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Aurora, CO (United States)

Citations

IDCFRDescription
337521 CFR 820.198(e)Records of complaint investigation
47921 CFR 820.50Purchasing controls, Lack of or inadequate procedures