FDA Inspection 1229084 — Corixa Corporation

Corixa Corporation — FEI 3007726770

The FDA completed an inspection of Corixa Corporation on February 9, 2024 in Marietta, PA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 3 citations were issued during this inspection. Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
February 9, 2024
Fiscal Year
2024
Product Type
Biologics
Project Area
Vaccines and Allergenic Products
Location
Marietta, PA (United States)

Citations

IDCFRDescription
127021 CFR 211.68(b)input/output verification
201421 CFR 211.188(b)(2)Identification of Equipment and Lines
922521 CFR 606.171Biological product deviation report