FDA Inspection 1041724 — Medtimo Inc

Medtimo Inc — FEI 3013508647

The FDA completed an inspection of Medtimo Inc on Feb 15, 2018 in Eden Prairie, MN. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Feb 15, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Eden Prairie, MN (United States)

Citations

IDCFRDescription
369621 CFR 820.100(b)Documentation
73121 CFR 803.50(a)(1)Report of Death or Serious Injury