# FDA Inspection 983344 - Avantis Medical - March 10, 2016

Source: https://www.keypedia.com/records/fda_inspections/avantis-medical/8cd68743-16f4-4aae-8caa-785d61138eff
Source feed: FDA_Inspections

> FDA Inspection 983344 for Avantis Medical on March 10, 2016. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 983344
- Company Name: Avantis Medical
- Inspection Date: 2016-03-10
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 983344 - 2016-03-10](https://www.keypedia.com/records/fda_inspections/avantis-medical/c9f71a18-2b7c-4366-89d8-e20758ba51c6)
- [FDA Inspection 785019 - 2012-06-08](https://www.keypedia.com/records/fda_inspections/avantis-medical/7b09986f-3d0a-4359-98e5-575ba1e6e700)
- [FDA Inspection 785019 - 2012-06-08](https://www.keypedia.com/records/fda_inspections/avantis-medical/1b2144c3-593e-40c4-8904-e9e31a6c0e61)
- [FDA Inspection 620295 - 2009-07-24](https://www.keypedia.com/records/fda_inspections/avantis-medical/517ae3a9-3ef4-4bd4-9a87-7b2f5fed435b)

Company: https://www.keypedia.com/companies/avantis-medical/535ad3e5-2cdd-47e6-aca1-def83ab3050e

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