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FDA Inspection 621212 — Wyeth Farma SA

Wyeth Farma SA — FEI 3003973260

The FDA completed an inspection of Wyeth Farma SA on September 25, 2009 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: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
September 25, 2009
Fiscal Year
2009
Product Type
Biologics
Project Area
Human Cellular, Tissue, and Gene Therapies
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))
  • 955103 (VAI Fri Dec 18 2015 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))

FDA data resources