FDA Inspection 738791 — American Homepatient Inc

American Homepatient Inc — FEI 1938040

The FDA completed an inspection of American Homepatient Inc on August 10, 2011 in Crystal City, MO. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
August 10, 2011
Fiscal Year
2011
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Crystal City, MO (United States)