FDA Inspection
Corixa CorporationCorixa Corporation – FDA Inspection, Feb 9, 2024
Record Details
This FDA Inspection record concerns Corixa Corporation, with an inspection on February 9, 2024, issued by the Center for Biologics Evaluation and Research, covering biologics.
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ID · 91f1c34e-f8ed-43de-852d-ffc1870c7427
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1229084
- FDA center
- Biologics
- Project area
- Vaccines and Allergenic Products
FDA Citations
3- 21 CFR 606.171Biological product deviation report
- 21 CFR 211.68(b)input/output verification
- 21 CFR 211.188(b)(2)Identification of Equipment and Lines
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Other FDA inspections of Corixa Corporation
4| Date | Classification | Office | Project area |
|---|---|---|---|
| March 12, 2026 | Not classified | Philadelphia District Office | Vaccine, Allergenic, and Live Biotherapeutic Products |
| April 15, 2019 | VAI | Center for Biologics Evaluation and Research | Vaccines and Allergenic Products |
| May 16, 2017 | VAI | Center for Biologics Evaluation and Research | Vaccines and Allergenic Products |
| May 13, 2015 | VAI | Center for Biologics Evaluation and Research | Vaccines and Allergenic Products |
Other documents for Corixa Corporation
- FDA Inspection 1298224 - 2026-03-12
- FDA Inspection 1091132 - 2019-04-15
- FDA Inspection 1016267 - 2017-05-16
- FDA Inspection 938930 - 2015-05-13
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