Home / Inspections / 1178127

FDA Inspection 1178127 — Wyeth Lederle S.r.l

Wyeth Lederle S.r.l — FEI 3002806766

The FDA completed an inspection of Wyeth Lederle S.r.l on January 21, 2022 in Catania. 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
January 21, 2022
Fiscal Year
2022
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Catania (Italy)

Additional Details

Mutual Recognition Agreement (MRA)

Facility

Other inspections at this facility

  • 1012188 (VAI Thu Apr 20 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 903600 (OAI Fri Nov 14 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 792624 (OAI Fri Jul 20 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 637083 (NAI Fri Dec 04 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources