FDA Inspection 728549 — Vitalant

Vitalant — FEI 2970045

The FDA completed an inspection of Vitalant on June 8, 2011 in Fairfield, 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 8, 2011
Fiscal Year
2011
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Fairfield, CA (United States)