# FDA Inspection 1062620 - Aeon Astron Europe B.V. - July 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 for Aeon Astron Europe B.V. on July 19, 2018. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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