FDA Inspection 1032319 — LEO Pharma Ireland
The FDA completed an inspection of LEO Pharma Ireland on Nov 3, 2017 in Dublin 12. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Nov 3, 2017
- Fiscal Year
- 2018
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Dublin 12 (Ireland)