FDA Inspection 1295446 — AstraZeneca AB

AstraZeneca AB — FEI 3003342394

The FDA completed an inspection of AstraZeneca AB on Nov 13, 2025 in Sodertalje. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Nov 13, 2025
Fiscal Year
2026
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Sodertalje (Sweden)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.