# FDA Inspection 949462 - LumiQuick Diagnostics Inc. - November 17, 2015

Source: https://www.keypedia.com/records/fda_inspections/lumiquick-diagnostics-inc/2d658d19-598c-4064-b13a-64dc7432fecb
Source feed: FDA_Inspections

> FDA Inspection 949462 for LumiQuick Diagnostics Inc. on November 17, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 949462
- Company Name: LumiQuick Diagnostics Inc.
- Inspection Date: 2015-11-17
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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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