FDA Inspection 1034676 — American HomePatient

American HomePatient — FEI 3004924741

The FDA completed an inspection of American HomePatient on November 17, 2017 in Collinsville, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Food/Cosmetics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
November 17, 2017
Fiscal Year
2018
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Collinsville, IL (United States)