FDA Inspection 726081 — Vitalant

Vitalant — FEI 1000143480

The FDA completed an inspection of Vitalant on April 28, 2011 in Aberdeen, SD. 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
April 28, 2011
Fiscal Year
2011
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Aberdeen, SD (United States)