FDA Inspection 852226 — Vitalant

Vitalant — FEI 1000121186

The FDA completed an inspection of Vitalant on October 22, 2013 in Coraopolis, 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
October 22, 2013
Fiscal Year
2014
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Coraopolis, PA (United States)