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FDA Inspection
•Novo Nordisk US Bio Production Inc.•December 9, 2025

Novo Nordisk US Bio Production Inc. – FDA Inspection, Dec 9, 2025

Record Details

This FDA Inspection record concerns Novo Nordisk US Bio Production Inc., with an inspection on December 9, 2025, issued by the New England District Office, covering human drugs.

Company
Novo Nordisk US Bio Production Inc.
Inspection Date
December 9, 2025
Product Type
Human Drugs
Office
New England District Office
People
  • Raihan A. Chowdhury (Issuing Officer)
  • Simone E. Pitts (FDA Associated Person)
  • Vivin George (Investigator)
View Company Profile

ID · b0077115-b9ef-46ae-81a7-75debc87bcbd

Inspection Facts

Inspection number
1292060
FDA center
Human Drugs
Outcome
Form 483 issued, view the record

Other FDA inspections of Novo Nordisk US Bio Production Inc.

3
DateClassificationOfficeProject area
March 5, 2025NAICenter for Biologics Evaluation and ResearchBlood and Blood Products
July 25, 2023VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
August 24, 2018Not classifiedNew England District Office
Other documents for Novo Nordisk US Bio Production Inc.
  • FDA Inspection 1255809 - 2025-03-05
  • FDA Inspection 1214482 - 2023-07-25
  • FDA Inspection 1064794 - 2018-08-24

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