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FDA Inspection
•Novo Nordisk A/S - G8, X9 M.FI•April 17, 2026

Novo Nordisk A/S - G8, X9 M.FI – FDA Inspection, Apr 17, 2026

Record Details

This FDA Inspection record concerns Novo Nordisk A/S - G8, X9 M.FI, with an inspection on April 17, 2026, issued by the Office of Inspections and Investigations, covering human drugs.

Company
Novo Nordisk A/S - G8, X9 M.FI
Inspection Date
April 17, 2026
Product Type
Human Drugs
Office
Office of Inspections and Investigations
Person
  • Ruben C. Ayala (Company Rep)
View Company Profile

ID · db3fab11-abbb-487e-b474-adf67f6e209f

Inspection Facts

Inspection number
1316850
FDA center
Human Drugs
Outcome
Form 483 issued, view the record

Other FDA inspections of Novo Nordisk A/S - G8, X9 M.FI

6
DateClassificationOfficeProject area
June 16, 2022VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
May 12, 2021VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
June 1, 2018NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
April 14, 2016NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
March 14, 2014VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 6 other inspections on the company page
Other documents for Novo Nordisk A/S - G8, X9 M.FI
  • FDA Inspection 1297668 - 2022-06-16
  • FDA Inspection 1210000 - 2021-05-12
  • FDA Inspection 1057701 - 2018-06-01
  • FDA Inspection 965339 - 2016-04-14
  • FDA Inspection 874067 - 2014-03-14

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