FDA Inspection 904925 — 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 Jul 23, 2014 in Sanford, NC. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Biologics.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Jul 23, 2014
Fiscal Year
2014
Product Type
Biologics
Project Area
Vaccines and Allergenic Products
Location
Sanford, NC (United States)

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