FDA Inspection 763981 — Immunex Rhode Island Corporation

Immunex Rhode Island Corporation — FEI 3003359885

The FDA completed an inspection of Immunex Rhode Island Corporation on Jan 20, 2012 in West Greenwich, RI. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection details

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

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