FDA Inspection 1089686 — Vitalant

Vitalant — FEI 2970085

The FDA completed an inspection of Vitalant on March 29, 2019 in Santa Rosa, 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
March 29, 2019
Fiscal Year
2019
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Santa Rosa, CA (United States)