FDA Inspection 1106094 — Vitalant

Vitalant — FEI 1771461

The FDA completed an inspection of Vitalant on September 20, 2019 in Billings, MT. 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 20, 2019
Fiscal Year
2019
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Billings, MT (United States)