FDA Inspection 941875 — Vitalant

Vitalant — FEI 2970030

The FDA completed an inspection of Vitalant on September 11, 2015 in Yuba City, 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 11, 2015
Fiscal Year
2015
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Yuba City, CA (United States)