FDA Inspection 996034 — Vitalant

Vitalant — FEI 2970618

The FDA completed an inspection of Vitalant on December 5, 2016 in San Mateo, 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 5, 2016
Fiscal Year
2017
Product Type
Biologics
Project Area
Blood and Blood Products
Location
San Mateo, CA (United States)