FDA Inspection
Novo Nordisk A/SNovo Nordisk A/S – FDA Inspection, Dec 5, 2019
Record Details
This FDA Inspection record concerns Novo Nordisk A/S, with an inspection on December 5, 2019, issued by the Center for Drug Evaluation and Research, covering drugs.
- Company
- Novo Nordisk A/S
- Inspection Date
- December 5, 2019
- Product Type
- Drugs
View Company Profile
ID · 1b2e0386-bb32-4a1e-b8c0-6bda25e404ad
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1165895
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
Other FDA inspections of Novo Nordisk A/S
8| Date | Classification | Office | Project area |
|---|---|---|---|
| March 29, 2023 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| May 18, 2018 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| February 8, 2017 | VAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| April 8, 2016 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| September 3, 2013 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Novo Nordisk A/S
- FDA Inspection 1245306 - 2023-03-29
- FDA Inspection 1057438 - 2018-05-18
- FDA Inspection 1007260 - 2017-02-08
- FDA Inspection 964462 - 2016-04-08
- FDA Inspection 846713 - 2013-09-03
Document or profile
One record shows the event. A profile shows the pattern.
Buy this document for the source file and details behind this single event.
Choose full profile access to connect related records, sites, people, citations, and enforcement history in one view.