FDA Inspection 771859 - K. W. Griffen Company DBA Biomed Packaging Systems - February 28, 2012
FDA Inspection 771859 for K. W. Griffen Company DBA Biomed Packaging Systems on February 28, 2012. Classification: Voluntary Action Indicated (VAI).
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FDA Inspection 771859 for K. W. Griffen Company DBA Biomed Packaging Systems on February 28, 2012. Classification: Voluntary Action Indicated (VAI).
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Inspection Date
February 28, 2012
Product Type
Drugs
ID: f74a0988-4c33-4313-8595-b1015a2cf300
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