# FDA Inspection 952747 - Haven Innovation, Inc. - December 17, 2015

Source: https://www.keypedia.com/records/fda_inspections/haven-innovation-inc/37e39c5f-34d8-4972-8783-0a2d6799c7aa
Source feed: FDA_Inspections

> FDA Inspection 952747 for Haven Innovation, Inc. on December 17, 2015. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 952747
- Company Name: Haven Innovation, Inc.
- Inspection Date: 2015-12-17
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 952747 - 2015-12-17](https://www.keypedia.com/records/fda_inspections/haven-innovation-inc/4b9bcb3d-1037-4874-bd44-d9daa7927176)
- [FDA Inspection 902887 - 2014-11-12](https://www.keypedia.com/records/fda_inspections/haven-innovation-inc/3420db52-4f86-4a9f-82cc-9732003c56e5)
- [FDA Inspection 871793 - 2014-03-27](https://www.keypedia.com/records/fda_inspections/haven-innovation-inc/2964254f-90e9-48e8-b054-9fe8f1c299bd)
- [FDA Inspection 781196 - 2012-05-02](https://www.keypedia.com/records/fda_inspections/haven-innovation-inc/f4047567-a6e6-406d-bb39-7268d199abf3)

Company: https://www.keypedia.com/companies/haven-innovation-inc/b261d153-5029-4383-b997-41f79f4ba3fe

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