FDA Inspection 808297 — American HomePatient

American HomePatient — FEI 3004924741

The FDA completed an inspection of American HomePatient on November 27, 2012 in Collinsville, IL. 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
November 27, 2012
Fiscal Year
2013
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Collinsville, IL (United States)