FDA Inspection 1275115 — AstraZeneca Dunkerque Production (AZDP)

AstraZeneca Dunkerque Production (AZDP) — FEI 3003063819

The FDA completed an inspection of AstraZeneca Dunkerque Production (AZDP) on Feb 3, 2022 in Dordogne. 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: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Feb 3, 2022
Fiscal Year
2022
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Dordogne (France)

Additional Details

Mutual Recognition Agreement (MRA)

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