FDA Inspection 857602 — Vitalant

Vitalant — FEI 3005619551

The FDA completed an inspection of Vitalant on December 4, 2013 in Pittsburgh, PA. 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
December 4, 2013
Fiscal Year
2014
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Pittsburgh, PA (United States)