# Renovo Life LLC – FDA Inspection, Jan 26, 2018

Source: https://www.keypedia.com/records/fda_inspections/renovo-life-llc/2973a70a-70d6-4fc6-b643-9b69f28ad90f
Source feed: FDA_Inspections

> FDA inspection 1038739 of Renovo Life LLC, January 26, 2018. Classification: No Action Indicated (NAI). 3 citations under 21 CFR part 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1038739
- Company Name: Renovo Life LLC
- Inspection Date: 2018-01-26
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/gamal-a-norton/6b52c9e6-d579-4994-81ee-e734eb1f0a67)

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

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