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FDA Inspection 1097256 — Kub Technologies, Inc.

Kub Technologies, Inc. — FEI 3006051164

The FDA completed an inspection of Kub Technologies, Inc. on July 16, 2019 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
July 16, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
Stratford, CT (United States)

Facility

Other inspections at this facility

  • 1234862 (NAI Thu Dec 19 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1002194 (NAI Thu Feb 23 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 833233 (NAI Fri May 17 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 635740 (VAI Fri Dec 18 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources