FDA Inspection 1028526 — Immunex Rhode Island Corporation

Immunex Rhode Island Corporation — FEI 3003359885

The FDA completed an inspection of Immunex Rhode Island Corporation on Jul 17, 2017 in West Greenwich, RI. 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
Jul 17, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
West Greenwich, RI (United States)

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