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FDA Inspection
•Novo Nordisk A/S - 25a-B•November 7, 2023

FDA Inspection 1223821 - Novo Nordisk A/S - 25a-B - November 07, 2023

Record Details

This FDA Inspection record concerns Novo Nordisk A/S - 25a-B, with an inspection on November 7, 2023, issued by the Office of Inspections and Investigations.

Company
Novo Nordisk A/S - 25a-B
Inspection Date
November 7, 2023
Office
Office of Inspections and Investigations
Person
  • Laurimer Kuilan-Torres (Issuing Officer)
View Company Profile

ID · 1311c640-239f-42db-a99a-a4b693406f50

Inspection Facts

Inspection number
1223821
FDA center
Human Drugs
Outcome
Form 483 issued

Other FDA inspections of Novo Nordisk A/S - 25a-B

7
DateClassificationOfficeProject area
November 4, 2022VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
June 14, 2018VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
January 22, 2016VAICenter for Biologics Evaluation and ResearchBlood and Blood Products
June 18, 2015NAICenter for Devices and Radiological HealthCompliance: Devices
October 10, 2014NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 7 other inspections on the company page
Other documents for Novo Nordisk A/S - 25a-B
  • FDA Inspection 1207487 - 2022-11-04
  • FDA Inspection 1118196 - 2018-06-14
  • FDA Inspection 957571 - 2016-01-22
  • FDA Inspection 933969 - 2015-06-18
  • FDA Inspection 909374 - 2014-10-10

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