FDA Inspection 1058490 — Vitalant

Vitalant — FEI 1776382

The FDA completed an inspection of Vitalant on Jun 20, 2018 in Casper, WY. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jun 20, 2018
Fiscal Year
2018
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Casper, WY (United States)