# Advalight ApS – FDA Inspection, Apr 11, 2024

Source: https://www.keypedia.com/records/fda_inspections/advalight-aps/d6645aab-d9ba-420f-be63-e4932f45ef8e
Source feed: FDA_Inspections

> FDA inspection 1235694 of Advalight ApS, April 11, 2024. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1235694
- Company Name: Advalight ApS
- Inspection Date: 2024-04-11
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- [FDA Inspection 1049187 - 2018-04-19](https://www.keypedia.com/records/fda_inspections/advalight-aps/49277c5d-6048-46e7-a9ce-02d295b4b592)
- FDA Inspection 950736 - 2015-11-26

## Related Officers

- [Investigator](https://www.keypedia.com/people/jude-c-dike/ea760122-1121-420a-9875-c49de6f3bb0e)

Company: https://www.keypedia.com/companies/advalight-aps/a67b50d1-6457-422c-ae66-d15e2aa1369b

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