FDA Inspection 759148 — Vitalant

Vitalant — FEI 2077785

The FDA completed an inspection of Vitalant on December 14, 2011 in Santa Maria, 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
December 14, 2011
Fiscal Year
2012
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Santa Maria, CA (United States)