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FDA Inspection
•Octapharma AB•October 3, 2016

Octapharma AB – FDA Inspection, Oct 3, 2016

Record Details

This FDA Inspection record concerns Octapharma AB, with an inspection on October 3, 2016, issued by the Office of Inspections and Investigations, covering biologics.

Company
Octapharma AB
Inspection Date
October 3, 2016
Product Type
Biologics
Office
Office of Inspections and Investigations
People
  • Cynthia Jim (FDA Associated Person)
  • Debra M. Emerson (FDA Associated Person)
View Company Profile

ID · 6b3e378f-099f-4e8b-a570-ba2acbf16cb8

Inspection Facts

Inspection number
994537
FDA center
Biologics
Outcome
Form 483 issued

Other FDA inspections of Octapharma AB

6
DateClassificationOfficeProject area
September 19, 2023VAICenter for Biologics Evaluation and ResearchBlood and Blood Products
September 28, 2018VAICenter for Biologics Evaluation and ResearchBlood and Blood Products
April 28, 2014VAICenter for Biologics Evaluation and ResearchBlood and Blood Products
January 19, 2012VAICenter for Biologics Evaluation and ResearchBlood and Blood Products
January 20, 2011OAICenter for Biologics Evaluation and ResearchBlood and Blood Products
View all 6 other inspections on the company page
Other documents for Octapharma AB
  • FDA Inspection 1218250 - 2023-09-19
  • FDA Inspection 1070173 - 2018-09-28
  • FDA Inspection 894095 - 2014-04-28
  • FDA Inspection 783783 - 2012-01-19
  • FDA Inspection 710676 - 2011-01-20

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