# FDA Inspection 1038739 - Renovo Life LLC - January 26, 2018

Source: https://www.globalkeysolutions.net/records/fda_inspections/renovo-life-llc/0e842a7a-8197-4643-ae88-19e35b180890
Source feed: FDA_Inspections

> FDA Inspection 1038739 for Renovo Life LLC on January 26, 2018. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1038739
- Company Name: Renovo Life LLC
- Inspection Date: 2018-01-26
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1038739 - 2018-01-26](https://www.globalkeysolutions.net/records/fda_inspections/renovo-life-llc/2973a70a-70d6-4fc6-b643-9b69f28ad90f)

Company: https://www.globalkeysolutions.net/companies/renovo-life-llc/4d99de9a-bf1e-4675-a238-2dfcda0880d0

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