# FDA Inspection 1295738 - LumiQuick Diagnostics Inc. - November 05, 2025

Source: https://www.keypedia.com/records/fda_inspections/lumiquick-diagnostics-inc/bb595299-45f5-4fb7-8216-89812e19452a
Source feed: FDA_Inspections

> FDA Inspection 1295738 for LumiQuick Diagnostics Inc. on November 05, 2025. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1295738
- Company Name: LumiQuick Diagnostics Inc.
- Inspection Date: 2025-11-05
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1295738 - 2025-11-05](https://www.keypedia.com/records/fda_inspections/lumiquick-diagnostics-inc/a8a6cdfe-5ce8-4158-92e8-0175d5927431)
- [FDA Inspection 1295738 - 2025-11-05](https://www.keypedia.com/records/fda_inspections/lumiquick-diagnostics-inc/5fdc1c5d-2914-4b54-8233-02abebff9606)
- [FDA Inspection 949462 - 2015-11-17](https://www.keypedia.com/records/fda_inspections/lumiquick-diagnostics-inc/79ebbe48-bb5d-4051-89ec-c78f02d95969)
- [FDA Inspection 949462 - 2015-11-17](https://www.keypedia.com/records/fda_inspections/lumiquick-diagnostics-inc/2d658d19-598c-4064-b13a-64dc7432fecb)
- [FDA Inspection 935468 - 2015-07-24](https://www.keypedia.com/records/fda_inspections/lumiquick-diagnostics-inc/bf85368d-3a07-4627-a3e4-9387e3678b0b)

Company: https://www.keypedia.com/companies/lumiquick-diagnostics-inc/04511435-12aa-4d1d-8902-602abcd2ca12

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7