FDA Inspection 1295446 — AstraZeneca AB

AstraZeneca AB — FEI 3003342394

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

Inspection Details

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