FDA Inspection 1076937 — Vitalant

Vitalant — FEI 3002572707

The FDA completed an inspection of Vitalant on Dec 19, 2018 in Oak Lawn, 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
Dec 19, 2018
Fiscal Year
2019
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Oak Lawn, IL (United States)