FDA Inspection 1162569 — Vitalant

Vitalant — FEI 3016436029

The FDA completed an inspection of Vitalant on February 18, 2022 in Brisbane, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
February 18, 2022
Fiscal Year
2022
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Brisbane, CA (United States)

Citations

IDCFRDescription
6721 CFR 606.65(e)Following manufacturer's instructions