FDA Inspection 984109 — Vitalant

Vitalant — FEI 3007101464

The FDA completed an inspection of Vitalant on August 18, 2016 in Mather, 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 18, 2016
Fiscal Year
2016
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Mather, CA (United States)