FDA Inspection 1227529 — VitalDyne, Inc

VitalDyne, Inc — FEI 3003697998

The FDA completed an inspection of VitalDyne, Inc on Dec 21, 2023 in Cokato, 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
Dec 21, 2023
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
Cokato, MN (United States)