FDA Inspection 951010 — Vitalant

Vitalant — FEI 1421612

The FDA completed an inspection of Vitalant on November 24, 2015 in Arlington Heights, IL. 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
November 24, 2015
Fiscal Year
2016
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Arlington Heights, IL (United States)