FDA Inspection 899256 — Vitalant

Vitalant — FEI 3000205813

The FDA completed an inspection of Vitalant on October 8, 2014 in Middleburg Heights, OH. 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 8, 2014
Fiscal Year
2015
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Middleburg Heights, OH (United States)