FDA Inspection 801077 — AstraZeneca AB

AstraZeneca AB — FEI 3003342394

The FDA completed an inspection of AstraZeneca AB on May 29, 2012 in Sodertalje. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
May 29, 2012
Fiscal Year
2012
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Sodertalje (Sweden)

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