FDA Inspection 958214 — Vitalant

Vitalant — FEI 2973165

The FDA completed an inspection of Vitalant on Jan 28, 2016 in San Francisco, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jan 28, 2016
Fiscal Year
2016
Product Type
Biologics
Project Area
Blood and Blood Products
Location
San Francisco, CA (United States)