FDA Inspection 867516 — Vitalant

Vitalant — FEI 2571073

The FDA completed an inspection of Vitalant on March 4, 2014 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
March 4, 2014
Fiscal Year
2014
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Pittsburgh, PA (United States)

Citations

IDCFRDescription
15421 CFR 606.160(a)(1)Concurrent documentation