FDA Inspection 1305396 — 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 Apr 23, 2026 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). 1 citation was issued during this inspection. Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Apr 23, 2026
Fiscal Year
2026
Product Type
Biologics
Project Area
Vaccines and Allergenic Products
Location
Sanford, NC (United States)

Citations

IDCFRDescription
356121 CFR 211.56(b)Written sanitation procedures lacking

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