FDA Inspection 680914 — Biogen, Inc.

Biogen, Inc. — FEI 1220951

The FDA completed an inspection of Biogen, Inc. on Sep 8, 2010 in Cambridge, MA. 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
Sep 8, 2010
Fiscal Year
2010
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Cambridge, MA (United States)

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