FDA Inspection 1219696 — AstraZeneca Pharmaceuticals LP

AstraZeneca Pharmaceuticals LP — FEI 2518137

The FDA completed an inspection of AstraZeneca Pharmaceuticals LP on September 20, 2023 in Wilmington, DE. 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
September 20, 2023
Fiscal Year
2023
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Wilmington, DE (United States)

Additional Details

Postmarket Adverse Drug Experience (PADE)