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FDA Inspection 1295738 — LumiQuick Diagnostics Inc.

LumiQuick Diagnostics Inc. — FEI 3005984081

The FDA completed an inspection of LumiQuick Diagnostics Inc. on November 5, 2025 in Santa Clara, CA. 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
November 5, 2025
Fiscal Year
2026
Product Type
Devices
Project Area
Compliance: Devices
Location
Santa Clara, CA (United States)

Facility

Other inspections at this facility

  • 949462 (NAI Tue Nov 17 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 935468 (VAI Fri Jul 24 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 867537 (NAI Mon Feb 24 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 809900 (OAI Fri Dec 07 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources