FDA Inspection 1101508 — Vitalant

Vitalant — FEI 1000522999

The FDA completed an inspection of Vitalant on September 6, 2019 in Davis, 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
September 6, 2019
Fiscal Year
2019
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Davis, CA (United States)