FDA Inspection 854838 — Vitalant

Vitalant — FEI 2970085

The FDA completed an inspection of Vitalant on November 1, 2013 in Santa Rosa, 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
November 1, 2013
Fiscal Year
2014
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Santa Rosa, CA (United States)