# Aeon Astron Europe B.V. – FDA Inspection, Jul 19, 2018

Source: https://www.keypedia.com/records/fda_inspections/aeon-astron-europe-bv/a38e7caa-36b0-4d8f-9164-2bfe2b9d8176
Source feed: FDA_Inspections

> FDA inspection 1062620 of Aeon Astron Europe B.V., July 19, 2018. Classification: Voluntary Action Indicated (VAI). 4 citations under 21 CFR part 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1062620
- Company Name: Aeon Astron Europe B.V.
- Inspection Date: 2018-07-19
- 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: 4

## Related Officers

- [Company Rep](https://www.keypedia.com/people/joseph-d-gong/c1079a56-5f84-4e0d-9f76-9dc1187e588a)

Company: https://www.keypedia.com/companies/aeon-astron-europe-bv/9ed3e04f-3f58-414a-93d2-c1b40eb8aaf4

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