FDA Inspection 794892 - German Newall, MD - August 09, 2012
FDA Inspection 794892 for German Newall, MD on August 09, 2012. Classification: Voluntary Action Indicated (VAI).
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FDA Inspection 794892 for German Newall, MD on August 09, 2012. Classification: Voluntary Action Indicated (VAI).
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Company
German Newall, MDInspection Date
August 9, 2012
Product Type
Devices
ID: fd26c5af-3ddb-4b23-a063-ea7669c9e1ad
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