FDA Inspection 1062136 — Vitalant

Vitalant — FEI 2970030

The FDA completed an inspection of Vitalant on July 10, 2018 in Yuba City, 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
July 10, 2018
Fiscal Year
2018
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Yuba City, CA (United States)