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FDA Inspection 1028526 — Immunex Rhode Island Corporation

Immunex Rhode Island Corporation — FEI 3003359885

The FDA completed an inspection of Immunex Rhode Island Corporation on July 17, 2017 in West Greenwich, RI. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
July 17, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
West Greenwich, RI (United States)

Facility

Other inspections at this facility

  • 1324094 (NAI Wed Jun 03 2026 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1191233 (NAI Thu Oct 27 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 890647 (NAI Thu Aug 07 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 763981 (VAI Fri Jan 20 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 597685 (NAI Fri Jun 19 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources