FDA Inspection 1015469 - Alber GmbH - May 11, 2017

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Record Details

This FDA Inspection record concerns Alber GmbH, with an inspection on May 11, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: Alber GmbH
Inspection Date: May 11, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · cd031c4f-54d1-408d-a0bd-a557c0dddecf

Violation Codes4

21 CFR 820.100(a)21 CFR 820.198(a)21 CFR 820.30(g)21 CFR 820.30(i)

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