# FDA Inspection 944713 - Ellipse A/S - September 18, 2015

Source: https://www.keypedia.com/records/fda_inspections/ellipse-as/3e02f44d-30d6-4ab9-aaa7-e1572d64d2bb
Source feed: FDA_Inspections

> FDA Inspection 944713 for Ellipse A/S on September 18, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 944713
- Company Name: Ellipse A/S
- Inspection Date: 2015-09-18
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 944713 - 2015-09-18](https://www.keypedia.com/records/fda_inspections/ellipse-as/44e5a136-6d36-401b-b05f-8afcd15dc6c5)
- [FDA Inspection 833130 - 2013-05-31](https://www.keypedia.com/records/fda_inspections/ellipse-as/c039acb1-3dae-49cc-99f8-8051c06c2549)
- [FDA Inspection 833130 - 2013-05-31](https://www.keypedia.com/records/fda_inspections/ellipse-as/50f9c42c-e67e-45f1-bdaf-98e71cbde355)
- [FDA Inspection 833130 - 2013-05-31](https://www.keypedia.com/records/fda_inspections/ellipse-as/5a2c1c5e-6f63-4381-b7bc-cccef588142c)

Company: https://www.keypedia.com/companies/ellipse-as/6f774955-8964-4099-b0ac-f9461acc923e

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