# P-Ryton Corp – FDA Inspection, Dec 6, 2012

Source: https://www.keypedia.com/records/fda_inspections/p-ryton-corp/834eaaea-b72f-4c57-a6ce-bf312853aa3a
Source feed: FDA_Inspections

> FDA inspection 809812 of P-Ryton Corp, December 06, 2012. Classification: Voluntary Action Indicated (VAI). 5 citations under 21 CFR part 820. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 809812
- Company Name: P-Ryton Corp
- Inspection Date: 2012-12-06
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 5

## Related Documents

- FDA Inspection 919338 - 2015-03-24
- [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