FDA Inspection 871163 — Vitalant

Vitalant — FEI 1000515229

The FDA completed an inspection of Vitalant on March 24, 2014 in Lansing, IL. 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 24, 2014
Fiscal Year
2014
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Lansing, IL (United States)