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FDA Inspection
•Amo Groningen BV•November 13, 2019

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

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Record Details

This FDA Inspection record concerns Amo Groningen BV, with an inspection on November 13, 2019, issued by the Center for Devices and Radiological Health, covering devices.

Company
Amo Groningen BV
Inspection Date
November 13, 2019
Product Type
Devices
Office
Center for Devices and Radiological Health
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ID · fabbbf0e-836f-4493-b131-c84f57a69756

Violation Codes1
21 CFR 820.90(a)

Full citation text and observation details available on the Dashboard.

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