FDA Inspection 1078439 — Vitalant

Vitalant — FEI 1421612

The FDA completed an inspection of Vitalant on November 27, 2018 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 27, 2018
Fiscal Year
2019
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Arlington Heights, IL (United States)