FDA Inspection
PENTAPHARM AGFDA 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.
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ID · a6fc0494-430a-4e6d-be89-beab1b7af213
Violation Codes1
21 CFR 820.100(a)
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