FDA Inspection 918326 — Vitalant

Vitalant — FEI 1000124022

The FDA completed an inspection of Vitalant on March 6, 2015 in Placerville, 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
March 6, 2015
Fiscal Year
2015
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Placerville, CA (United States)