FDA Inspection 1080662 — BioLife Plasma Services
The FDA completed an inspection of BioLife Plasma Services on Feb 6, 2019 in Mount Juliet, TN. 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 6, 2019
- Fiscal Year
- 2019
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Mount Juliet, TN (United States)