FDA Inspection 1098166 — Vitalant

Vitalant — FEI 3007101464

The FDA completed an inspection of Vitalant on July 18, 2019 in Mather, 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 18, 2019
Fiscal Year
2019
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Mather, CA (United States)