FDA Inspection 988595 - PENTAPHARM AG - September 15, 2016

Record Details

This FDA Inspection record concerns PENTAPHARM AG, with an inspection on September 15, 2016, issued by the Center for Devices and Radiological Health, covering devices.

Company: PENTAPHARM AG
Inspection Date: September 15, 2016
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · a6fc0494-430a-4e6d-be89-beab1b7af213

Violation Codes1

21 CFR 820.100(a)

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