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FDA Inspection 652853 — Wyeth Pharmaceutical Division of Wyeth Holdings LLC

Wyeth Pharmaceutical Division of Wyeth Holdings LLC — FEI 1000110954

The FDA completed an inspection of Wyeth Pharmaceutical Division of Wyeth Holdings LLC on December 11, 2009 in Sanford, NC. 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
December 11, 2009
Fiscal Year
2010
Product Type
Biologics
Project Area
Vaccines and Allergenic Products
Location
Sanford, NC (United States)

Facility

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FDA data resources