FDA Inspection 605948 - Reinemann, Edward & Son, Inc - August 20, 2009
FDA Inspection 605948 for Reinemann, Edward & Son, Inc on August 20, 2009. Classification: No Action Indicated (NAI).
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FDA Inspection 605948 for Reinemann, Edward & Son, Inc on August 20, 2009. Classification: No Action Indicated (NAI).
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Company
Reinemann, Edward & Son, IncInspection Date
August 20, 2009
Product Type
Veterinary
ID: f679adf7-9620-4354-8b24-a4ed5f778546
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