FDA Inspection 798352 — Vitalant

Vitalant — FEI 1421612

The FDA completed an inspection of Vitalant on September 12, 2012 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
September 12, 2012
Fiscal Year
2012
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Arlington Heights, IL (United States)