# FDA Inspection 969947 - US Defib Medical Technologies, LLC - February 09, 2016

Source: https://www.keypedia.com/records/fda_inspections/us-defib-medical-technologies-llc/04bee2ee-b961-411a-b3de-576bd4d0768d
Source feed: FDA_Inspections

> FDA Inspection 969947 for US Defib Medical Technologies, LLC on February 09, 2016. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 969947
- Company Name: US Defib Medical Technologies, LLC
- Inspection Date: 2016-02-09
- 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 969947 - 2016-02-09](https://www.keypedia.com/records/fda_inspections/us-defib-medical-technologies-llc/e58b5421-e39a-4d18-a2dc-baada0f783a3)

Company: https://www.keypedia.com/companies/us-defib-medical-technologies-llc/6b79306c-fc94-4259-8803-a1100efc1a4e

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