# FDA Inspection 919338 - P-Ryton Corp - March 24, 2015

Source: https://www.keypedia.com/records/fda_inspections/p-ryton-corp/4b4c57e8-ba89-4f55-8132-e8f646eb8035
Source feed: FDA_Inspections

> FDA Inspection 919338 for P-Ryton Corp on March 24, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 919338
- Company Name: P-Ryton Corp
- Inspection Date: 2015-03-24
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 919338 - 2015-03-24](https://www.keypedia.com/records/fda_inspections/p-ryton-corp/9b87987b-90ff-436a-86ce-2d2575b3417c)
- [FDA Inspection 809812 - 2012-12-06](https://www.keypedia.com/records/fda_inspections/p-ryton-corp/834eaaea-b72f-4c57-a6ce-bf312853aa3a)
- [FDA Inspection 809812 - 2012-12-06](https://www.keypedia.com/records/fda_inspections/p-ryton-corp/3aa59ede-eb24-4b90-a98f-25103e1f4de7)
- [FDA Inspection 729278 - 2011-06-10](https://www.keypedia.com/records/fda_inspections/p-ryton-corp/4cffe406-2a43-461b-99d0-40c9e2917e89)
- [FDA Inspection 571849 - 2009-04-01](https://www.keypedia.com/records/fda_inspections/p-ryton-corp/6e3419f8-dd33-4328-a8ff-4344bd479a4d)

Company: https://www.keypedia.com/companies/p-ryton-corp/223a8a10-609a-47cd-8f86-f609021b9d00

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