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FDA Inspection 818295 — Padagis US LLC

Padagis US LLC — FEI 2127022

The FDA completed an inspection of Padagis US LLC on February 6, 2013 in Minneapolis, MN. 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
February 6, 2013
Fiscal Year
2013
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Minneapolis, MN (United States)

Facility

Other inspections at this facility

  • 1304064 (VAI Wed Apr 08 2026 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1248645 (VAI Fri Sep 06 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1228870 (NAI Wed Jan 31 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1207462 (NAI Fri May 05 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1162776 (VAI Fri Feb 18 2022 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources