FDA Inspection 1254088 — Lek d.d.

Lek d.d. — FEI 3002807460

The FDA completed an inspection of Lek d.d. on December 11, 2023 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
December 11, 2023
Fiscal Year
2024
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Ljubljana (Slovenia)

Additional Details

Mutual Recognition Agreement (MRA)