FDA Inspection 1062620 - Aeon Astron Europe B.V. - July 19, 2018

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Record Details

This FDA Inspection record concerns Aeon Astron Europe B.V., with an inspection on July 19, 2018, issued by the Center for Devices and Radiological Health, covering devices.

Company: Aeon Astron Europe B.V.
Inspection Date: July 19, 2018
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · a38e7caa-36b0-4d8f-9164-2bfe2b9d8176

Violation Codes4

21 CFR 820.100(a)21 CFR 820.198(a)21 CFR 820.25(b)21 CFR 820.80(b)

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