FDA Inspection 965124 - Biotronik SE & Co. KG - March 10, 2016

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Record Details

This FDA Inspection record concerns Biotronik SE & Co. KG, with an inspection on March 10, 2016, issued by the Center for Devices and Radiological Health, covering devices.

Company: Biotronik SE & Co. KG
Inspection Date: March 10, 2016
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · a4d3498b-6107-4a3e-a86a-bf074b50ed71

Violation Codes6

21 CFR 803.50(a)(2)21 CFR 820.250(b)21 CFR 820.30(c)21 CFR 820.50(a)(1)21 CFR 820.70(c)21 CFR 820.75(a)

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