FDA Inspection 1050839 — Genzyme Ireland Limited

Genzyme Ireland Limited — FEI 3003809840

The FDA completed an inspection of Genzyme Ireland Limited on Feb 16, 2018 in Waterford. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Feb 16, 2018
Fiscal Year
2018
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Waterford (Ireland)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.