# FDA Inspection 858562 - Prexion, Inc. - December 26, 2013

Source: https://www.keypedia.com/records/fda_inspections/prexion-inc/03e00ac8-75ab-40a0-bf3a-38f5b134a609
Source feed: FDA_Inspections

> FDA Inspection 858562 for Prexion, Inc. on December 26, 2013. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 858562
- Company Name: Prexion, Inc.
- Inspection Date: 2013-12-26
- 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 1064537 - 2018-08-22](https://www.keypedia.com/records/fda_inspections/prexion-inc/617880a0-0871-438f-a781-1455887cf22d)
- [FDA Inspection 858562 - 2013-12-26](https://www.keypedia.com/records/fda_inspections/prexion-inc/6ab7d6a1-f391-4152-a4fa-3ac9899804a8)

Company: https://www.keypedia.com/companies/prexion-inc/40eca2ec-413d-40c3-85c3-0654259d3f46

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