# FDA Inspection 709564 - Neoventa Medical AB - February 10, 2011

Source: https://www.keypedia.com/records/fda_inspections/neoventa-medical-ab/85a2389e-0319-4798-99b5-7b470f495250
Source feed: FDA_Inspections

> FDA Inspection 709564 for Neoventa Medical AB on February 10, 2011. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 709564
- Company Name: Neoventa Medical AB
- Inspection Date: 2011-02-10
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 709564 - 2011-02-10](https://www.keypedia.com/records/fda_inspections/neoventa-medical-ab/f3ec349d-ca6e-4290-8b00-fa38a23c7c12)
- [FDA Inspection 658312 - 2010-04-01](https://www.keypedia.com/records/fda_inspections/neoventa-medical-ab/863ee3e7-8abf-4a0a-af4f-1851dff22ce4)
- [FDA Inspection 658312 - 2010-04-01](https://www.keypedia.com/records/fda_inspections/neoventa-medical-ab/4b894499-6010-408e-9e1c-7f51506a24e8)

Company: https://www.keypedia.com/companies/neoventa-medical-ab/1f21c969-6c75-4fed-aebb-de581adc2e4e

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