Immunex Corp.

FDA Regulatory Profile

Immunex Corp. has 0 FDA recalls, 1 inspection, 0 510(k) clearances and 0 compliance actions on record.

What these totals cover: FDA records filed under the name "Immunex Corp." and its spelling variant "Immunex". They do not include records filed under Amgen or other names in its corporate family; those are listed under Related names, each with its own counts.

Latest inspection
Oct 17, 2008 · NAI

Newer recall under related name Amgen: Jun 4, 2026, D-0616-2026.

Part of the Amgen corporate family.

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 8, 2026File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections1Nov 13, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA inspections

1 inspection on Oct 17, 2008.

DateSiteProductClassificationFEI
Oct 17, 2008Thousand Oaks, CADrugsNo Action Indicated (NAI)1000125884
NAI
No objectionable conditions or practices were found during the inspection.
VAI
Objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action.
OAI
Regulatory and/or administrative actions are recommended.

Look up the inspector observations behind these results with the FDA 483 search, or check for formal enforcement with the FDA warning letter search.

FDA-inspected facilities

1 inspected site, newest inspection first.

FacilityLocationInspectionsLatest
FEI 1000125884Thousand Oaks, CA1Oct 17, 2008

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Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.