FDA Inspection 1069768 — Vitalant

Vitalant — FEI 3014398502

The FDA completed an inspection of Vitalant on October 22, 2018 in Neptune, NJ. 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
October 22, 2018
Fiscal Year
2019
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Neptune, NJ (United States)