FDA Inspection 991333 — Univar USA Inc

Univar USA Inc — FEI 2125935

The FDA completed an inspection of Univar USA Inc on Oct 25, 2016 in Saint Paul, MN. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Oct 25, 2016
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Saint Paul, MN (United States)