# FDA Inspection 814361 - Resonetics, LLC - January 16, 2013

Source: https://www.keypedia.com/records/fda_inspections/resonetics-llc/e9725a09-9933-4e7e-9915-16cda5d47125
Source feed: FDA_Inspections

> FDA Inspection 814361 for Resonetics, LLC on January 16, 2013. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 814361
- Company Name: Resonetics, LLC
- Inspection Date: 2013-01-16
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 970299 - 2016-05-03](https://www.keypedia.com/records/fda_inspections/resonetics-llc/28ae421d-95a2-4691-b301-55a2d3e7bf72)
- [FDA Inspection 970299 - 2016-05-03](https://www.keypedia.com/records/fda_inspections/resonetics-llc/0b7f95d2-a272-489c-8fd3-ae680594ce25)

Company: https://www.keypedia.com/companies/resonetics-llc/12602bc9-f96f-4148-9e72-98d04ff01ece

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