FDA Inspection 785881 — LEK d.d.
The FDA completed an inspection of LEK d.d. on May 17, 2012 in Prevalje. 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
- May 17, 2012
- Fiscal Year
- 2012
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Prevalje (Slovenia)