# FDA Inspection 824190 - Lumedx - March 20, 2013

Source: https://www.keypedia.com/records/fda_inspections/lumedx/22351b33-76e0-478c-8cca-eec480a5260a
Source feed: FDA_Inspections

> FDA Inspection 824190 for Lumedx on March 20, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 824190
- Company Name: Lumedx
- Inspection Date: 2013-03-20
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 824190 - 2013-03-20](https://www.keypedia.com/records/fda_inspections/lumedx/1918c815-f952-4574-9ffd-17f93cd93bb3)
- [FDA Inspection 741045 - 2011-08-24](https://www.keypedia.com/records/fda_inspections/lumedx/4dbd6107-510f-4ecc-ab30-52ada2e16b75)

Company: https://www.keypedia.com/companies/lumedx/d8651cd8-3292-4842-aab4-d40cae56f918

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