FDA Inspection 977621 — Haleon Ireland Dungarvan Limited
The FDA completed an inspection of Haleon Ireland Dungarvan Limited on Jun 10, 2016 in Dungarvan. 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
- Jun 10, 2016
- Fiscal Year
- 2016
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Dungarvan (Ireland)