FDA Inspection 732562 — Vitalant

Vitalant — FEI 1000123568

The FDA completed an inspection of Vitalant on June 30, 2011 in Auburn, CA. 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
June 30, 2011
Fiscal Year
2011
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Auburn, CA (United States)