FDA Inspection 1178973 — Lek D.D.

Lek D.D. — FEI 3002807460

The FDA completed an inspection of Lek D.D. on Mar 18, 2022 in Ljubljana. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Mar 18, 2022
Fiscal Year
2022
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Ljubljana (Slovenia)

Additional Details

Mutual Recognition Agreement (MRA)