FDA Inspection 1234862 — Kub Technologies, Inc.

Kub Technologies, Inc. — FEI 3006051164

The FDA completed an inspection of Kub Technologies, Inc. on December 19, 2024 in Stratford, CT. 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 19, 2024
Fiscal Year
2025
Product Type
Devices
Project Area
Radiation Control and Health Safety Act
Location
Stratford, CT (United States)