FDA Inspection 1093195 — Bioreliance Ltd.
The FDA completed an inspection of Bioreliance Ltd. on Mar 15, 2019 in Glasgow. 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
- Mar 15, 2019
- Fiscal Year
- 2019
- Product Type
- Biologics
- Project Area
- Vaccines and Allergenic Products
- Location
- Glasgow (United Kingdom)