FDA Inspection 1300160 — Veranova LP

Veranova LP — FEI 2245277

The FDA completed an inspection of Veranova LP on January 23, 2026 in West Deptford, NJ. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
January 23, 2026
Fiscal Year
2026
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
West Deptford, NJ (United States)