FDA Inspection 1129231 — AstraZeneca UK Ltd.

AstraZeneca UK Ltd. — FEI 3002850317

The FDA completed an inspection of AstraZeneca UK Ltd. on Feb 23, 2020 in Macclesfield. 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 23, 2020
Fiscal Year
2020
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Macclesfield (United Kingdom)

Additional details

Mutual Recognition Agreement (MRA)

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