FDA Inspection 988048 — Vitalant
The FDA completed an inspection of Vitalant on September 16, 2016 in San Luis Obispo, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.
Inspection Details
- Classification
- No Action Indicated (NAI) (NAI)
- End Date
- September 16, 2016
- Fiscal Year
- 2016
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- San Luis Obispo, CA (United States)