FDA Inspection 1246916 — Lek d.d.

Lek d.d. — FEI 3002807460

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

Additional Details

Bioanalytical BA/BE