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FDA Inspection 1081817 — Veranova LP

Veranova LP — FEI 2245277

The FDA completed an inspection of Veranova LP on March 8, 2019 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
March 8, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
West Deptford, NJ (United States)

Facility

Other inspections at this facility

  • 1300160 (VAI Fri Jan 23 2026 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1197654 (VAI Wed Feb 15 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1040846 (VAI Wed Jan 31 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 968447 (NAI Thu May 05 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 853338 (NAI Thu Oct 31 2013 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources