FDA Inspection 1016280 — Biogen MA Inc.

Biogen MA Inc. — FEI 3000719749

The FDA completed an inspection of Biogen MA Inc. on March 23, 2017 in Morrisville, NC. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
March 23, 2017
Fiscal Year
2017
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Morrisville, NC (United States)