FDA Inspection 607529 — Univar Solutions

Univar Solutions — FEI 1000118256

The FDA completed an inspection of Univar Solutions on Aug 26, 2009 in Omaha, NE. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 2 citations were issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Aug 26, 2009
Fiscal Year
2009
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Omaha, NE (United States)

Citations

IDCFRDescription
176721 CFR 211.137(a)Expiration date lacking
191421 CFR 211.166(a)Lack of written stability program