FDA Inspection 1129231 — AstraZeneca UK Ltd.

AstraZeneca UK Ltd. — FEI 3002850317

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

Additional Details

Mutual Recognition Agreement (MRA)