# FDA Inspection 957605 - EXALT DEVICES LLC - January 08, 2016

Source: https://www.keypedia.com/records/fda_inspections/exalt-devices-llc/920da0a8-8917-4fa3-b2b3-4ba01056a63d
Source feed: FDA_Inspections

> FDA Inspection 957605 for EXALT DEVICES LLC on January 08, 2016. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 957605
- Company Name: EXALT DEVICES LLC
- Inspection Date: 2016-01-08
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 957605 - 2016-01-08](https://www.keypedia.com/records/fda_inspections/exalt-devices-llc/785bb7a5-81aa-47f5-8e62-274b552a3d5f)

Company: https://www.keypedia.com/companies/exalt-devices-llc/b309f09d-34c3-4429-bb1a-c910d798008f

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