FDA Inspection 1191869 — Lonza AG

Lonza AG — FEI 3014753648

The FDA completed an inspection of Lonza AG on Nov 4, 2022 in Basel Town. 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
Nov 4, 2022
Fiscal Year
2023
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Basel Town (Switzerland)