# Rigicon AS – FDA Inspection, Feb 15, 2023

Source: https://www.keypedia.com/records/fda_inspections/rigicon-as/b1208f36-d513-42dd-855f-04c38b9ea450
Source feed: FDA_Inspections

> FDA inspection 1197439 of Rigicon AS, February 15, 2023. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1197439
- Company Name: Rigicon AS
- Inspection Date: 2023-02-15
- 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: 2

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/brian-s-keefer/4fec578b-ca72-4d79-8634-3a9fe7ecd9a5)

Company: https://www.keypedia.com/companies/rigicon-as/e945391a-8190-4da1-b69a-ef2ff0895801

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