FDA Inspection 839238 — AstraZeneca Dunkerque Production (AZDP)

AstraZeneca Dunkerque Production (AZDP) — FEI 3003063819

The FDA completed an inspection of AstraZeneca Dunkerque Production (AZDP) on May 17, 2013 in Dordogne. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
May 17, 2013
Fiscal Year
2013
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Dordogne (France)

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