FDA Inspection 853825 - Advanced Sterilization Products - November 15, 2013
FDA Inspection 853825 for Advanced Sterilization Products on November 15, 2013. Classification: Voluntary Action Indicated (VAI).
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FDA Inspection 853825 for Advanced Sterilization Products on November 15, 2013. Classification: Voluntary Action Indicated (VAI).
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Inspection Date
November 15, 2013
Product Type
Devices
ID: faa60cba-2566-4d0f-b707-28d8f7e109c0
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