FDA Inspection 1234339 — NaviNetics, Inc.

NaviNetics, Inc. — FEI 3023194190

The FDA completed an inspection of NaviNetics, Inc. on Mar 13, 2024 in Rochester, 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
Mar 13, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Rochester, MN (United States)