FDA Inspection 844627 — Vitalant

Vitalant — FEI 1000124022

The FDA completed an inspection of Vitalant on August 15, 2013 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
August 15, 2013
Fiscal Year
2013
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Placerville, CA (United States)