FDA Inspection 1031660 - Bioptron AG - November 01, 2017

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Record Details

This FDA Inspection record concerns Bioptron AG, with an inspection on November 1, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: Bioptron AG
Inspection Date: November 1, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 07f1c13f-6f11-4006-a120-2fe91af93781

Violation Codes5

21 CFR 820.18421 CFR 820.250(b)21 CFR 820.70(i)21 CFR 820.72(a)21 CFR 820.90(b)(2)

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