FDA Inspection 868880 — Vitalant

Vitalant — FEI 2970030

The FDA completed an inspection of Vitalant on March 3, 2014 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
March 3, 2014
Fiscal Year
2014
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Yuba City, CA (United States)