FDA Inspection 981931 - NARVA Lichtquelle GmbH + Co. KG - July 29, 2016

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Record Details

This FDA Inspection record concerns NARVA Lichtquelle GmbH + Co. KG, with an inspection on July 29, 2016, issued by the Center for Devices and Radiological Health, covering devices.

Company: NARVA Lichtquelle GmbH + Co. KG
Inspection Date: July 29, 2016
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 75391140-14cc-406f-b29d-0f06c400ee45

Violation Codes10

21 CFR 820.100(a)21 CFR 820.18121 CFR 820.198(a)21 CFR 820.2221 CFR 820.30(a)21 CFR 820.40(b)21 CFR 820.70(f)21 CFR 820.72(b)21 CFR 820.8621 CFR 820.90(a)

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