FDA Inspection 897345 — Vitalant

Vitalant — FEI 2077785

The FDA completed an inspection of Vitalant on September 24, 2014 in Santa Maria, 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 24, 2014
Fiscal Year
2014
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Santa Maria, CA (United States)