FDA Inspection 1119496 — Vitalant

Vitalant — FEI 1471533

The FDA completed an inspection of Vitalant on Feb 6, 2020 in Schaumburg, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Feb 6, 2020
Fiscal Year
2020
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Schaumburg, IL (United States)