FDA Inspection 1041771 — Hovione Limited

Hovione Limited — FEI 3008058822

The FDA completed an inspection of Hovione Limited on Dec 22, 2017 in Ringaskiddy. 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
Dec 22, 2017
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Ringaskiddy (Ireland)