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FDA Inspection 1119381 — Actavis Italy Spa A Socio Unico

Actavis Italy Spa A Socio Unico — FEI 3001116953

The FDA completed an inspection of Actavis Italy Spa A Socio Unico on May 24, 2019 in Nerviano. 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
May 24, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Nerviano (Italy)

Additional Details

Mutual Recognition Agreement (MRA)

Facility

Other inspections at this facility

  • 1083251 (VAI Fri Mar 15 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1010790 (NAI Tue Dec 06 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 942841 (VAI Fri Sep 18 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 850924 (VAI Fri Sep 27 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 741518 (NAI Fri Jul 22 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources