# FDA Inspection 631944 - Argen Corporation, The - November 18, 2009

Source: https://www.keypedia.com/records/fda_inspections/argen-corporation-the/102bff87-b80e-4ad0-9444-6da8d0154ddf
Source feed: FDA_Inspections

> FDA Inspection 631944 for Argen Corporation, The on November 18, 2009. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 631944
- Company Name: Argen Corporation, The
- Inspection Date: 2009-11-18
- Classification: No Action Indicated (NAI)
- 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 859122 - 2013-12-12](https://www.keypedia.com/records/fda_inspections/argen-corporation-the/d3f5d4d8-dfbc-4c08-be29-8d956361fcc6)

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
