FDA Inspection 984392 — AstraZeneca Pharmaceuticals LP

AstraZeneca Pharmaceuticals LP — FEI 3011604962

The FDA completed an inspection of AstraZeneca Pharmaceuticals LP on Mar 10, 2016 in Denver, CO. 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
Mar 10, 2016
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Denver, CO (United States)

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