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FDA Inspection 987003 — Argenta US Manufacturing LLC

Argenta US Manufacturing LLC — FEI 1910953

The FDA completed an inspection of Argenta US Manufacturing LLC on August 15, 2016 in Shawnee, KS. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
August 15, 2016
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Shawnee, KS (United States)

Facility

Other inspections at this facility

  • 1225274 (VAI Fri Dec 15 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1192756 (VAI Wed Dec 14 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1182235 (VAI Fri Oct 28 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1098756 (VAI Thu Aug 01 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 936339 (VAI Thu Jul 30 2015 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources