FDA Inspection 732650 - American HomePatient Inc - June 28, 2011
FDA Inspection 732650 for American HomePatient Inc on June 28, 2011. Classification: No Action Indicated (NAI).
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FDA Inspection 732650 for American HomePatient Inc on June 28, 2011. Classification: No Action Indicated (NAI).
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Company
American HomePatient IncInspection Date
June 28, 2011
Product Type
Drugs
ID: fc1ecd84-6d4e-44d4-8ab4-7a683d08785c
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