FDA Inspection 999732 — Vitalant
The FDA completed an inspection of Vitalant on Dec 7, 2016 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
- Dec 7, 2016
- Fiscal Year
- 2017
- Product Type
- Biologics
- Project Area
- Blood and Blood Products
- Location
- Elk Grove, CA (United States)