# FDA Inspection 824899 - P4X, Inc. - March 29, 2013

Source: https://www.keypedia.com/records/fda_inspections/p4x-inc/40485b65-d48e-45cd-a12e-8794986d8c13
Source feed: FDA_Inspections

> FDA Inspection 824899 for P4X, Inc. on March 29, 2013. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 824899
- Company Name: P4X, Inc.
- Inspection Date: 2013-03-29
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 824899 - 2013-03-29](https://www.keypedia.com/records/fda_inspections/p4x-inc/c05c722c-ce0e-44dd-b649-90a610fd67c6)
- [FDA Inspection 570916 - 2009-03-18](https://www.keypedia.com/records/fda_inspections/p4x-inc/2c276365-de30-4db5-b7b8-a57e75a580ed)
- [FDA Inspection 570916 - 2009-03-18](https://www.keypedia.com/records/fda_inspections/p4x-inc/175ddfba-6b96-4916-9a25-790be327094c)

Company: https://www.keypedia.com/companies/p4x-inc/1b169f7d-4ef5-4edc-9e74-b6b122d98acf

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