FDA Inspection 750368 — Haleon Ireland Dungarvan Limited

Haleon Ireland Dungarvan Limited — FEI 3003721894

The FDA completed an inspection of Haleon Ireland Dungarvan Limited on Sep 22, 2011 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
Sep 22, 2011
Fiscal Year
2011
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Dungarvan (Ireland)