# FDA Inspection 894093 - Pro-Dex Inc - September 05, 2014

Source: https://www.keypedia.com/records/fda_inspections/pro-dex-inc/2264ee99-e01a-4fa7-a9e4-c93aa199b3f9
Source feed: FDA_Inspections

> FDA Inspection 894093 for Pro-Dex Inc on September 05, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 894093
- Company Name: Pro-Dex Inc
- Inspection Date: 2014-09-05
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 894093 - 2014-09-05](https://www.keypedia.com/records/fda_inspections/pro-dex-inc/06e7256f-004a-49eb-9fae-5e7f332097fc)
- [FDA Inspection 752142 - 2011-10-12](https://www.keypedia.com/records/fda_inspections/pro-dex-inc/c98c651b-5080-4944-b643-7776d9d16617)
- [FDA Inspection 752142 - 2011-10-12](https://www.keypedia.com/records/fda_inspections/pro-dex-inc/3033c3ae-17b9-445d-afe8-d7b461b46154)

Company: https://www.keypedia.com/companies/pro-dex-inc/a3fa5ead-48d6-4f7a-ac6b-2f5c92b0dea1

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