FDA Inspection 620103 — Vitalant
The FDA completed an inspection of Vitalant on Jun 2, 2009 in Elk Grove, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Jun 2, 2009
- Fiscal Year
- 2009
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Elk Grove, CA (United States)