FDA Inspection 1049261 — Genzyme Flanders

Genzyme Flanders — FEI 3003623839

The FDA completed an inspection of Genzyme Flanders on Mar 23, 2018 in Geel. 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
Mar 23, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Geel (Belgium)