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FDA Inspection 757334 — AstraZeneca Nijmegen B.V.

AstraZeneca Nijmegen B.V. — FEI 3003000472

The FDA completed an inspection of AstraZeneca Nijmegen B.V. on September 27, 2011 in Nijmegen. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
September 27, 2011
Fiscal Year
2011
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Nijmegen (Netherlands)

Facility

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FDA data resources