FDA Inspection 1063664 — Vitalant

Vitalant — FEI 1776389

The FDA completed an inspection of Vitalant on July 27, 2018 in Bismarck, ND. 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 27, 2018
Fiscal Year
2018
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Bismarck, ND (United States)