FDA Inspection 1246916 — Lek D.D.

Lek D.D. — FEI 3002807460

The FDA completed an inspection of Lek D.D. on Jul 26, 2024 in Ljubljana. 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
Jul 26, 2024
Fiscal Year
2024
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Ljubljana (Slovenia)

Additional Details

Bioanalytical BA/BE