FDA Inspection 835859 — Medtimo Inc

Medtimo Inc — FEI 3013508647

The FDA completed an inspection of Medtimo Inc on Jun 4, 2013 in Eden Prairie, MN. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jun 4, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Eden Prairie, MN (United States)