FDA Inspection 1298224 — Corixa Corporation

Corixa Corporation — FEI 3007726770

The FDA completed an inspection of Corixa Corporation on March 12, 2026 in Marietta, 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 12, 2026
Fiscal Year
2026
Product Type
Biologics
Project Area
Vaccines and Allergenic Products
Location
Marietta, PA (United States)

Citations

IDCFRDescription
143421 CFR 211.42(c)(10)(iv)Environmental Monitoring System