FDA Inspection 1031661 - Bioptron AG - November 02, 2017

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Record Details

This FDA Inspection record concerns Bioptron AG, with an inspection on November 2, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: Bioptron AG
Inspection Date: November 2, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 64a6b3f7-060c-4ef5-8887-84acf699a633

Violation Codes10

21 CFR 1002.10(d)21 CFR 803.17(a)(1)21 CFR 820.100(a)21 CFR 820.198(a)21 CFR 820.200(d)21 CFR 820.2221 CFR 820.30(c)21 CFR 820.30(e)21 CFR 820.30(f)21 CFR 820.30(g)

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