FDA Inspection 826472 — Genzyme Corporation

Genzyme Corporation — FEI 3009389940

The FDA completed an inspection of Genzyme Corporation on Apr 9, 2013 in Northborough, MA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Apr 9, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
Northborough, MA (United States)

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