FDA Inspection 1029919 — Mckesson Drug Company

Mckesson Drug Company — FEI 1030548

The FDA completed an inspection of Mckesson Drug Company on Jul 28, 2017 in Duluth, GA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Food/Cosmetics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jul 28, 2017
Fiscal Year
2017
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Duluth, GA (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.