FDA Inspection 1096697 — Vitalant

Vitalant — FEI 1000139516

The FDA completed an inspection of Vitalant on June 12, 2019 in Las Cruces, 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 12, 2019
Fiscal Year
2019
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Las Cruces, NM (United States)