FDA Inspection 1144139 — Vitalant

Vitalant — FEI 1000139335

The FDA completed an inspection of Vitalant on June 14, 2021 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 14, 2021
Fiscal Year
2021
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Santa Fe, NM (United States)