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FDA Inspection
•Novo Nordisk A/S - G8, X9 M.FI•June 16, 2022

Novo Nordisk A/S - G8, X9 M.FI – FDA Inspection, Jun 16, 2022

Record Details

This FDA Inspection record concerns Novo Nordisk A/S - G8, X9 M.FI, with an inspection on June 16, 2022, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Novo Nordisk A/S - G8, X9 M.FI
Inspection Date
June 16, 2022
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · a73b5e51-19ef-492f-93ba-175b269567c1

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
1297668
FDA center
Human Drugs
Project area
Drug Quality Assurance

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

6
DateClassificationOfficeProject area
April 17, 2026Not classifiedOffice of Inspections and Investigations
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 1316850 - 2026-04-17
  • 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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