FDA Inspection 1028034 — Vitalant

Vitalant — FEI 1000139516

The FDA completed an inspection of Vitalant on July 21, 2017 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
July 21, 2017
Fiscal Year
2017
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Las Cruces, NM (United States)