# Retivue Llc – FDA Inspection, Apr 17, 2024

Source: https://www.keypedia.com/records/fda_inspections/retivue-llc/676e7d64-5853-4f6d-9dfa-385655622665
Source feed: FDA_Inspections

> FDA inspection 1236108 of Retivue Llc, April 17, 2024. Classification: Voluntary Action Indicated (VAI). 5 citations under 21 CFR part 820.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1236108
- Company Name: Retivue Llc
- Inspection Date: 2024-04-17
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 5

## Related Officers

- [Investigator](https://www.keypedia.com/people/heath-a-gerber/3c47dcdd-875c-4f3c-8165-839354a53d8b)

Company: https://www.keypedia.com/companies/retivue-llc/3c0d1167-b334-433c-bdb5-06b0e9f2cad2

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