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FDA Inspection 1220541 — Archimica S.p.A

Archimica S.p.A — FEI 3002874947

The FDA completed an inspection of Archimica S.p.A on June 15, 2023 in Lodi. 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
June 15, 2023
Fiscal Year
2023
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Lodi (Italy)

Additional Details

Mutual Recognition Agreement (MRA)

Facility

Other inspections at this facility

  • 1123733 (VAI Thu Sep 13 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1094988 (VAI Fri Jul 21 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1013470 (VAI Fri Apr 28 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 900514 (NAI Thu Sep 25 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 744980 (NAI Thu Sep 08 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources