FDA Inspection 897397 — Vitalant

Vitalant — FEI 1776382

The FDA completed an inspection of Vitalant on Sep 26, 2014 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
Sep 26, 2014
Fiscal Year
2014
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Casper, WY (United States)