FDA Inspection 1131957 — The Bartell Drug Company

The Bartell Drug Company — FEI 3006733580

The FDA completed an inspection of The Bartell Drug Company on September 24, 2020 in Des Moines, WA. 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
September 24, 2020
Fiscal Year
2020
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Des Moines, WA (United States)