FDA Inspection 919557 — Norco Inc

Norco Inc — FEI 1000151022

The FDA completed an inspection of Norco Inc on March 18, 2015 in Bend, OR. 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
March 18, 2015
Fiscal Year
2015
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Bend, OR (United States)

Citations

IDCFRDescription
438721 CFR 211.198(a)Reporting of adverse drug experience to FDA