FDA Inspection 893478 — Vitalant

Vitalant — FEI 2970045

The FDA completed an inspection of Vitalant on August 27, 2014 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
August 27, 2014
Fiscal Year
2014
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Fairfield, CA (United States)