FDA Inspection 753061 — Vitalant

Vitalant — FEI 2970030

The FDA completed an inspection of Vitalant on November 10, 2011 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
November 10, 2011
Fiscal Year
2012
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Yuba City, CA (United States)