FDA Inspection 994412 — Vitalant

Vitalant — FEI 3000205813

The FDA completed an inspection of Vitalant on December 14, 2016 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
December 14, 2016
Fiscal Year
2017
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Middleburg Heights, OH (United States)