Home / Inspections / 955103

FDA Inspection 955103 — Wyeth Farma SA

Wyeth Farma SA — FEI 3003973260

The FDA completed an inspection of Wyeth Farma SA on December 18, 2015 in San Sebastian De Los Reyes. 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
December 18, 2015
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
San Sebastian De Los Reyes (Spain)

Facility

Other inspections at this facility

  • 1115256 (VAI Fri Sep 27 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1032496 (VAI Tue Oct 03 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 876520 (NAI Fri Apr 04 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 874557 (VAI Thu Jan 30 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 755077 (VAI Wed Oct 12 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources