# FDA Inspection 787855 - Aribex Inc - June 20, 2012

Source: https://www.keypedia.com/records/fda_inspections/aribex-inc/8fbd68d2-0cdd-4274-a1a5-b5ca5d7e6664
Source feed: FDA_Inspections

> FDA Inspection 787855 for Aribex Inc on June 20, 2012. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 787855
- Company Name: Aribex Inc
- Inspection Date: 2012-06-20
- 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 787855 - 2012-06-20](https://www.keypedia.com/records/fda_inspections/aribex-inc/d1c45d30-9b19-4501-afe8-7dbc0dbd682f)

Company: https://www.keypedia.com/companies/aribex-inc/48f68e6b-de0d-4f25-9102-72450c33ec52

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