FDA Inspection 925013 — American Homepatient Inc

American Homepatient Inc — FEI 1931540

The FDA completed an inspection of American Homepatient Inc on May 5, 2015 in Kansas City, MO. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
May 5, 2015
Fiscal Year
2015
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Kansas City, MO (United States)