FDA Inspection 931958 - HP Halden Pharma AS - June 26, 2015
FDA Inspection 931958 for HP Halden Pharma AS on June 26, 2015. Classification: Voluntary Action Indicated (VAI).
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FDA Inspection 931958 for HP Halden Pharma AS on June 26, 2015. Classification: Voluntary Action Indicated (VAI).
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Company
HP Halden Pharma ASInspection Date
June 26, 2015
Product Type
Drugs
ID: d980d410-9dd9-440a-b669-0abda9c0f57c
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