FDA Inspection 918229 — Baxalta Belgium Manufacturing SA
The FDA completed an inspection of Baxalta Belgium Manufacturing SA on Feb 24, 2015 in Lessines. 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
- Feb 24, 2015
- Fiscal Year
- 2015
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Lessines (Belgium)