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483
•Novo Nordisk A/S - 25a-B•January 17, 2020

FDA 483 - Novo Nordisk A/S - 25a-B - January 17, 2020

Record Details

Novo Nordisk A/S, a control testing laboratory in Hillerod, Denmark, was cited for failing to conduct thorough investigations into unexplained discrepancies. The firm did not adequately investigate unknown peaks detected multiple times during HPLC analysis, leading to an insufficient root cause determination. This indicates a significant lapse in their quality control and deviation management systems.

Company
Novo Nordisk A/S - 25a-B
Inspection date
January 17, 2020
Product type
drugs
Office
Office of Biological Products Operations - Division I
People
  • Jean Cantillops
  • Sangeeta M. Khurana (Consumer Safety Officer)
View Company Profile

ID · 84ce6826-520f-4c13-83f3-58b02807c3d4

Other documents for Novo Nordisk A/S - 25a-B
  • 483 - 2023-11-07November 7, 2023
  • 483 - 2020-01-17January 17, 2020

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