FDA Inspection 1059379 - Haupt Pharma Muenster GmbH - July 06, 2018

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Record Details

This FDA Inspection record concerns Haupt Pharma Muenster GmbH, with an inspection on July 6, 2018, issued by the Center for Drug Evaluation and Research, covering drugs.

Company: Haupt Pharma Muenster GmbH
Inspection Date: July 6, 2018
Product Type: Drugs
Office: Center for Drug Evaluation and Research

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ID · 4cba233f-342f-4540-b7e3-f0dff689c21f

Violation Codes3

21 CFR 211.100(a)21 CFR 211.22(d)21 CFR 211.68(b)

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