# FDA Inspection 897363 - Augusta Medical Systems, LLC - July 22, 2014

Source: https://www.keypedia.com/records/fda_inspections/augusta-medical-systems-llc/7eca5083-83ac-4ea2-bd73-4a82e31e26e7
Source feed: FDA_Inspections

> FDA Inspection 897363 for Augusta Medical Systems, LLC on July 22, 2014. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 897363
- Company Name: Augusta Medical Systems, LLC
- Inspection Date: 2014-07-22
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1066597 - 2018-04-23](https://www.keypedia.com/records/fda_inspections/augusta-medical-systems-llc/815fd0b7-4222-49e2-905e-526e712fee7b)
- [FDA Inspection 1066597 - 2018-04-23](https://www.keypedia.com/records/fda_inspections/augusta-medical-systems-llc/1b8d51cd-cd35-4c52-821a-ac300f7cd274)
- [FDA Inspection 748019 - 2011-09-23](https://www.keypedia.com/records/fda_inspections/augusta-medical-systems-llc/3838075e-867a-4da3-88d2-e7bb91e5cb96)

Company: https://www.keypedia.com/companies/augusta-medical-systems-llc/fa564157-9425-48b1-a6bf-b8208d24f809

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