FDA Inspection 1040747 — Vitalant

Vitalant — FEI 1721390

The FDA completed an inspection of Vitalant on January 26, 2018 in Boulder, CO. 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
January 26, 2018
Fiscal Year
2018
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Boulder, CO (United States)