FDA issued a Warning Letter to Wyeth Lederle S.p.A on 3/27/2013 for a previous inspection.
483 Wyeth Lederle S.r.l Apr 2017

483 Wyeth Lederle S.r.l Apr 2017

David Gomes FDA, Junho Pak FDA$119.00 - Available Now

FDA investigators audited the Wyeth Lederle S.r.l - Catania, Italy facility and issued inspectional observations (via FDA 483) on 20 Apr 2017.

Product details

  • Category: Human Drugs
  • Inspection end: 20 Apr 2017
  • Location: Catania, Italy
  • FEI: 3002806766
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