FDA Inspection 1112441 — AstraZeneca Nijmegen B.V.

AstraZeneca Nijmegen B.V. — FEI 3003000472

The FDA completed an inspection of AstraZeneca Nijmegen B.V. on September 10, 2019 in Nijmegen. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
September 10, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Nijmegen (Netherlands)