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FDA Inspection 958791 — Biogen, Inc.

Biogen, Inc. — FEI 1220951

The FDA completed an inspection of Biogen, Inc. on February 9, 2016 in Cambridge, MA. 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
February 9, 2016
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Cambridge, MA (United States)

Facility

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FDA data resources