FDA Inspection 1007887 — AstraZeneca AB

AstraZeneca AB — FEI 3003342394

The FDA completed an inspection of AstraZeneca AB on January 27, 2017 in Sodertalje. 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
January 27, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Sodertalje (Sweden)