FDA Inspection 933183 — Novo Nordisk Production Belgium SA
The FDA completed an inspection of Novo Nordisk Production Belgium SA on May 28, 2015 in Brussels. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Biologics.
Inspection details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- May 28, 2015
- Fiscal Year
- 2015
- Product Type
- Biologics
- Project Area
- Vaccines and Allergenic Products
- Location
- Brussels (Belgium)