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FDA Inspection 952359 — Vee Pak LLC

Vee Pak LLC — FEI 1421421

The FDA completed an inspection of Vee Pak LLC on December 21, 2015 in Countryside, IL. 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
December 21, 2015
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Countryside, IL (United States)

Facility

Other inspections at this facility

  • 1275687 (NAI Fri Jul 25 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1260897 (NAI Mon Apr 07 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1224900 (VAI Mon Dec 11 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 941667 (NAI Wed Jun 17 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 720111 (VAI Fri Mar 25 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources