FDA Inspection 1059997 — Vitalant

Vitalant — FEI 1000523276

The FDA completed an inspection of Vitalant on July 11, 2018 in Napa, 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 11, 2018
Fiscal Year
2018
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Napa, CA (United States)