FDA Inspection 1249533 — Iotamotion Inc

Iotamotion Inc — FEI 3021286080

The FDA completed an inspection of Iotamotion Inc on Sep 12, 2024 in Vadnais Heights, 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). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Sep 12, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
Vadnais Heights, MN (United States)

Citations

IDCFRDescription
330921 CFR 820.120(b)Examination for accuracy