FDA Inspection 661821 — Upsher-Smith Laboratories, LLC

Upsher-Smith Laboratories, LLC — FEI 1719991

The FDA completed an inspection of Upsher-Smith Laboratories, LLC on April 30, 2010 in Denver, CO. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
April 30, 2010
Fiscal Year
2010
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Denver, CO (United States)

Citations

IDCFRDescription
135821 CFR 211.100(b)SOPs not followed / documented