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FDA Inspection
•Biogen MA Inc.•December 23, 2016

Biogen MA Inc. – FDA Inspection, Dec 23, 2016

Record Details

This FDA Inspection record concerns Biogen MA Inc., with an inspection on December 23, 2016, issued by the Atlanta District Office, covering human drugs.

Company
Biogen MA Inc.
Inspection Date
December 23, 2016
Product Type
Human Drugs
Office
Atlanta District Office
People
  • Thuy T. Nguyen (FDA Associated Person)
  • Viviana R. Ramirez (Issuing Officer)
View Company Profile

ID · 63d1cd7c-ce1d-438e-9845-7e84a02d3ed8

Inspection Facts

Inspection number
999559
FDA center
Human Drugs
Outcome
Form 483 issued

Other FDA inspections of Biogen MA Inc.

12
DateClassificationOfficeProject area
July 12, 2024NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
February 15, 2019VAICenter for Biologics Evaluation and ResearchBlood and Blood Products
June 13, 2018NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
March 23, 2017VAICenter for Biologics Evaluation and ResearchBlood and Blood Products
January 15, 2016NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 12 other inspections on the company page
Other documents for Biogen MA Inc.
  • FDA Inspection 1252412 - 2024-07-12
  • FDA Inspection 1084879 - 2019-02-15
  • FDA Inspection 1066958 - 2018-06-13
  • FDA Inspection 1016280 - 2017-03-23
  • FDA Inspection 978930 - 2016-01-15

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