# FDA Inspection 1064537 - Prexion, Inc. - August 22, 2018

Source: https://www.keypedia.com/records/fda_inspections/prexion-inc/617880a0-0871-438f-a781-1455887cf22d
Source feed: FDA_Inspections

> FDA Inspection 1064537 for Prexion, Inc. on August 22, 2018. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1064537
- Company Name: Prexion, Inc.
- Inspection Date: 2018-08-22
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 858562 - 2013-12-26](https://www.keypedia.com/records/fda_inspections/prexion-inc/6ab7d6a1-f391-4152-a4fa-3ac9899804a8)
- [FDA Inspection 858562 - 2013-12-26](https://www.keypedia.com/records/fda_inspections/prexion-inc/03e00ac8-75ab-40a0-bf3a-38f5b134a609)

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