# FDA Inspection 781320 - Enovate Medical, LLC - April 26, 2012

Source: https://www.keypedia.com/records/fda_inspections/enovate-medical-llc/677136e0-462f-4b25-a838-88ae06935229
Source feed: FDA_Inspections

> FDA Inspection 781320 for Enovate Medical, LLC on April 26, 2012. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 781320
- Company Name: Enovate Medical, LLC
- Inspection Date: 2012-04-26
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 902309 - 2014-11-06](https://www.keypedia.com/records/fda_inspections/enovate-medical-llc/c5c6163c-cd1c-4eeb-a3cc-f838cb5c5e4d)
- [FDA Inspection 902309 - 2014-11-06](https://www.keypedia.com/records/fda_inspections/enovate-medical-llc/74bdd377-20ab-44be-98e2-aaa3fd5b55c6)

Company: https://www.keypedia.com/companies/enovate-medical-llc/8e8f2026-8b68-41fb-b38f-513ef5d57e0e

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