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FDA Inspection 1084879 — Biogen MA Inc.

Biogen MA Inc. — FEI 3000719749

The FDA completed an inspection of Biogen MA Inc. on February 15, 2019 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
February 15, 2019
Fiscal Year
2019
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Morrisville, NC (United States)

Facility

Other inspections at this facility

  • 1252412 (NAI Fri Jul 12 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1066958 (NAI Wed Jun 13 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1016280 (VAI Thu Mar 23 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 978930 (NAI Fri Jan 15 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 932852 (NAI Fri Jun 19 2015 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources