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FDA Inspection 637083 — Wyeth Lederle S.r.l

Wyeth Lederle S.r.l — FEI 3002806766

The FDA completed an inspection of Wyeth Lederle S.r.l on December 4, 2009 in Catania. 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
December 4, 2009
Fiscal Year
2010
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Catania (Italy)

Facility

Other inspections at this facility

  • 1178127 (VAI Fri Jan 21 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 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))

Recent compliance actions

FDA data resources