FDA Inspection 1111640 - Amo Groningen BV - November 13, 2019

FDA Inspection 1111640 for Amo Groningen BV on November 13, 2019. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1111640 for Amo Groningen BV on November 13, 2019. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 820.90(a)

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Record Information

Company

Amo Groningen BV

Inspection Date

November 13, 2019

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fabbbf0e-836f-4493-b131-c84f57a69756

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