# FDA Inspection 971061 - Argon Medical Devices Inc. - May 04, 2016

Source: https://www.keypedia.com/records/fda_inspections/argon-medical-devices-inc/101fa31e-784b-4d8e-b884-a5e6f333a0b8
Source feed: FDA_Inspections

> FDA Inspection 971061 for Argon Medical Devices Inc. on May 04, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 971061
- Company Name: Argon Medical Devices Inc.
- Inspection Date: 2016-05-04
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 971061 - 2016-05-04](https://www.keypedia.com/records/fda_inspections/argon-medical-devices-inc/0f16927c-8472-4683-bea4-c0582c42bfbf)
- [FDA Inspection 769247 - 2012-01-18](https://www.keypedia.com/records/fda_inspections/argon-medical-devices-inc/0fd19026-fc24-442b-9442-8435616fb5ff)
- [FDA Inspection 769247 - 2012-01-18](https://www.keypedia.com/records/fda_inspections/argon-medical-devices-inc/c367f7ad-2e37-48fe-a803-9cd78ff98c60)

Company: https://www.keypedia.com/companies/argon-medical-devices-inc/6b34deac-fa44-4ee4-a303-588782090aad

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