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FDA Inspection 566232 — AstraZeneca Pharmaceuticals LP

AstraZeneca Pharmaceuticals LP — FEI 1825662

The FDA completed an inspection of AstraZeneca Pharmaceuticals LP on January 29, 2009 in Mount Vernon, IN. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
January 29, 2009
Fiscal Year
2009
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Mount Vernon, IN (United States)

Facility

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FDA data resources