FDA Inspection 892569 — Vitalant

Vitalant — FEI 2070111

The FDA completed an inspection of Vitalant on August 22, 2014 in Santa Barbara, 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
August 22, 2014
Fiscal Year
2014
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Santa Barbara, CA (United States)