# FDA Inspection 1023770 - Avazzia, Inc - August 30, 2017

Source: https://www.keypedia.com/records/fda_inspections/avazzia-inc/4fa8f75c-c4d1-4abd-a0a5-f8fed8c04a9b
Source feed: FDA_Inspections

> FDA Inspection 1023770 for Avazzia, Inc on August 30, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1023770
- Company Name: Avazzia, Inc
- Inspection Date: 2017-08-30
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1023770 - 2017-08-30](https://www.keypedia.com/records/fda_inspections/avazzia-inc/2126c5ec-0341-4a25-918d-f979015265fa)
- [FDA Inspection 673136 - 2010-07-13](https://www.keypedia.com/records/fda_inspections/avazzia-inc/cad47a85-a02e-4195-8d63-6c57e67dfcdc)
- [FDA Inspection 673136 - 2010-07-13](https://www.keypedia.com/records/fda_inspections/avazzia-inc/9bbe336e-707d-4766-8c99-dbf9015ebff8)

Company: https://www.keypedia.com/companies/avazzia-inc/7fc3192e-2878-49e8-851a-e8cc52d4fefb

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