# FDA Inspection 1179340 - Rapid Reboot Recovery Products, LLC - September 08, 2022

Source: https://www.keypedia.com/records/fda_inspections/rapid-reboot-recovery-products-llc/a141cd42-8260-42d7-9907-250e8a2a5c20
Source feed: FDA_Inspections

> FDA Inspection 1179340 for Rapid Reboot Recovery Products, LLC on September 08, 2022. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1179340
- Company Name: Rapid Reboot Recovery Products, LLC
- Inspection Date: 2022-09-08
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1179340 - 2022-09-08](https://www.keypedia.com/records/fda_inspections/rapid-reboot-recovery-products-llc/030ac71e-ba58-440d-a055-d9b7db8b6200)
- [FDA Inspection 1073080 - 2018-11-29](https://www.keypedia.com/records/fda_inspections/rapid-reboot-recovery-products-llc/7c8ccc62-4248-4908-b655-ecd1ec3fb716)
- [FDA Inspection 1073080 - 2018-11-29](https://www.keypedia.com/records/fda_inspections/rapid-reboot-recovery-products-llc/85784388-eca3-4ab5-9eea-2a9fd2af7e88)

Company: https://www.keypedia.com/companies/rapid-reboot-recovery-products-llc/ce2aadd0-2ebf-455d-910d-2b548c130762

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