FDA Inspection 720111 — Vee Pak LLC

Vee Pak LLC — FEI 1421421

The FDA completed an inspection of Vee Pak LLC on March 25, 2011 in Countryside, IL. 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 25, 2011
Fiscal Year
2011
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Countryside, IL (United States)

Citations

IDCFRDescription
241921 CFR 211.198(a)Complaint Handling Procedure