FDA Inspection 932617 — Vitalant Reference and Transfusion Service

Vitalant Reference and Transfusion Service — FEI 3003329439

The FDA completed an inspection of Vitalant Reference and Transfusion Service on July 2, 2015 in Pittsburgh, PA. 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
July 2, 2015
Fiscal Year
2015
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Pittsburgh, PA (United States)

Citations

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