FDA Inspection 1119506 — Vitalant

Vitalant — FEI 2970045

The FDA completed an inspection of Vitalant on February 12, 2020 in Fairfield, CA. 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
February 12, 2020
Fiscal Year
2020
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Fairfield, CA (United States)