# FDA Inspection 859122 - Argen Corporation, The - December 12, 2013

Source: https://www.keypedia.com/records/fda_inspections/argen-corporation-the/d3f5d4d8-dfbc-4c08-be29-8d956361fcc6
Source feed: FDA_Inspections

> FDA Inspection 859122 for Argen Corporation, The on December 12, 2013. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 859122
- Company Name: Argen Corporation, The
- Inspection Date: 2013-12-12
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 859122 - 2013-12-12](https://www.keypedia.com/records/fda_inspections/argen-corporation-the/569a396f-7945-4c67-9416-18c782200c1b)
- [FDA Inspection 631944 - 2009-11-18](https://www.keypedia.com/records/fda_inspections/argen-corporation-the/102bff87-b80e-4ad0-9444-6da8d0154ddf)

Company: https://www.keypedia.com/companies/argen-corporation-the/dcd306eb-9aa4-45e3-8aeb-d90f0d80a1e1

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