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FDA Inspection 763981 — Immunex Rhode Island Corporation

Immunex Rhode Island Corporation — FEI 3003359885

The FDA completed an inspection of Immunex Rhode Island Corporation on January 20, 2012 in West Greenwich, RI. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
January 20, 2012
Fiscal Year
2012
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
West Greenwich, RI (United States)

Facility

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