FDA Inspection 637028 — Vitalant

Vitalant — FEI 3005619551

The FDA completed an inspection of Vitalant on January 6, 2010 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
January 6, 2010
Fiscal Year
2010
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Pittsburgh, PA (United States)