FDA Inspection 1095946 — Vitalant

Vitalant — FEI 1000139335

The FDA completed an inspection of Vitalant on June 4, 2019 in Santa Fe, NM. 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
June 4, 2019
Fiscal Year
2019
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Santa Fe, NM (United States)