FDA Inspection 903680 — Vitalant

Vitalant — FEI 1000123568

The FDA completed an inspection of Vitalant on November 4, 2014 in Auburn, 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 4, 2014
Fiscal Year
2015
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Auburn, CA (United States)