FDA Inspection 1069507 — Vitalant

Vitalant — FEI 1000139692

The FDA completed an inspection of Vitalant on October 22, 2018 in Rio Rancho, NM. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 1 citation was issued during this inspection. Product area: Biologics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
October 22, 2018
Fiscal Year
2019
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Rio Rancho, NM (United States)

Citations

IDCFRDescription
15521 CFR 606.160(b)Required records