FDA Inspection 1049077 — Vitalant

Vitalant — FEI 3012336081

The FDA completed an inspection of Vitalant on April 3, 2018 in Parker, CO. 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
April 3, 2018
Fiscal Year
2018
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Parker, CO (United States)