FDA Inspection 747381 — AstraZeneca Pharmaceuticals LP

AstraZeneca Pharmaceuticals LP — FEI 3004829714

The FDA completed an inspection of AstraZeneca Pharmaceuticals LP on May 3, 2011 in Philadelphia, PA. 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
May 3, 2011
Fiscal Year
2011
Product Type
Biologics
Project Area
Vaccines and Allergenic Products
Location
Philadelphia, PA (United States)

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