FDA Inspection 1015469 - Alber GmbH - May 11, 2017

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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