FDA Inspection 942228 — Vitalant

Vitalant — FEI 2976506

The FDA completed an inspection of Vitalant on September 16, 2015 in San Francisco, 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
September 16, 2015
Fiscal Year
2015
Product Type
Biologics
Project Area
Blood and Blood Products
Location
San Francisco, CA (United States)