FDA Inspection 1123337 — LEK d.d.
The FDA completed an inspection of LEK d.d. on March 14, 2019 in Prevalje. 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
- March 14, 2019
- Fiscal Year
- 2019
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Prevalje (Slovenia)
Additional Details
Mutual Recognition Agreement (MRA)