FDA Inspection 673657 — American Homepatient Inc

American Homepatient Inc — FEI 1931540

The FDA completed an inspection of American Homepatient Inc on Jul 28, 2010 in Kansas City, MO. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Jul 28, 2010
Fiscal Year
2010
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Kansas City, MO (United States)

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