FDA Inspection 1297634 — Novidan Inc

Novidan Inc — FEI 3015651976

The FDA completed an inspection of Novidan Inc on December 11, 2025 in Golden Valley, MN. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
December 11, 2025
Fiscal Year
2026
Product Type
Devices
Project Area
Compliance: Devices
Location
Golden Valley, MN (United States)