# FDA Inspection 809900 - LumiQuick Diagnostics Inc. - December 07, 2012

Source: https://www.globalkeysolutions.net/records/fda_inspections/lumiquick-diagnostics-inc/df045863-a951-4a3d-90b3-f5e3e2aae3b9
Source feed: FDA_Inspections

> FDA Inspection 809900 for LumiQuick Diagnostics Inc. on December 07, 2012. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 809900
- Company Name: LumiQuick Diagnostics Inc.
- Inspection Date: 2012-12-07
- Classification: Official Action Indicated (OAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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

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