FDA Inspection 1271780 — LEK Pharmaceuticals d.d.
The FDA completed an inspection of LEK Pharmaceuticals d.d. on November 24, 2022 in Lendava. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- November 24, 2022
- Fiscal Year
- 2023
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Lendava (Slovenia)
Additional Details
Mutual Recognition Agreement (MRA)