# FDA Inspection 581718 - Medtox Diagnostics, Inc. - May 06, 2009

Source: https://www.keypedia.com/records/fda_inspections/medtox-diagnostics-inc/20dae793-9c7e-4d52-93ce-d1d33f45b172
Source feed: FDA_Inspections

> FDA Inspection 581718 for Medtox Diagnostics, Inc. on May 06, 2009. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 581718
- Company Name: Medtox Diagnostics, Inc.
- Inspection Date: 2009-05-06
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1009293 - 2017-03-30](https://www.keypedia.com/records/fda_inspections/medtox-diagnostics-inc/5d06fa1d-159f-48c9-9313-9c26085980df)
- [FDA Inspection 581718 - 2009-05-06](https://www.keypedia.com/records/fda_inspections/medtox-diagnostics-inc/b91cb5d4-b814-4ad1-a174-1bd3934d85c7)

Company: https://www.keypedia.com/companies/medtox-diagnostics-inc/8a036a94-a8db-4f87-bb82-44b171b498df

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