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Avid Bioservices Inc.

FDA Regulatory Profile

Avid Bioservices Inc. has 0 FDA recalls, 7 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
May 29, 2025 · NAI

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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
Inspections7Nov 11, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
May 29, 2025Tustin, CADrugsNo Action Indicated (NAI)3003624288
Feb 1, 2018Tustin, CADrugsNo Action Indicated (NAI)3003624288
Mar 13, 2015Tustin, CADrugsNo Action Indicated (NAI)3003624288
Feb 8, 2013Tustin, CADrugsNo Action Indicated (NAI)3003624288
Apr 24, 2012Tustin, CADrugsVoluntary Action Indicated (VAI)3003624288
Apr 4, 2011Tustin, CADrugsVoluntary Action Indicated (VAI)3003624288
Jan 12, 2009Tustin, CADrugsNo Action Indicated (NAI)3003624288

NAI means no objectionable conditions or practices were found during the inspection. VAI means objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action. OAI means regulatory and/or administrative actions are recommended.

FDA-Inspected Facilities

FacilityLocationInspectionsLatest
FEI 3003624288Tustin, CA7May 29, 2025

FDA data resources

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