FDA Inspection 750412 — Vitalant

Vitalant — FEI 1000522998

The FDA completed an inspection of Vitalant on Oct 20, 2011 in Grass Valley, CA. 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
Oct 20, 2011
Fiscal Year
2012
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Grass Valley, CA (United States)