# FDA Inspection 1007155 - Medtox Diagnostics Inc - February 10, 2017

Source: https://www.keypedia.com/records/fda_inspections/medtox-diagnostics-inc/38d44112-fbf7-44e6-bb5f-bb204132b8fc
Source feed: FDA_Inspections

> FDA Inspection 1007155 for Medtox Diagnostics Inc on February 10, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1007155
- Company Name: Medtox Diagnostics Inc
- Inspection Date: 2017-02-10
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 831744 - 2012-12-13](https://www.keypedia.com/records/fda_inspections/medtox-diagnostics-inc/addba4ad-424e-4473-bf2e-1d5e8f1124b3)

Company: https://www.keypedia.com/companies/medtox-diagnostics-inc/f52edc39-202d-49fc-b10c-83869e894835

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