FDA Inspection 733852 - Octapharma Plasma, Inc. Portsmouth - June 28, 2011
FDA Inspection 733852 for Octapharma Plasma, Inc. Portsmouth on June 28, 2011. Classification: Voluntary Action Indicated (VAI).
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FDA Inspection 733852 for Octapharma Plasma, Inc. Portsmouth on June 28, 2011. Classification: Voluntary Action Indicated (VAI).
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Inspection Date
June 28, 2011
Product Type
Biologics
ID: ffecfff3-542f-4658-858f-176088ee823f
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