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Defender SD Manufacturing LLC

FDA Regulatory Profile

Defender SD Manufacturing LLC has 0 FDA recalls, 9 inspections, 0 510(k) clearances and 1 compliance action on record.

Latest inspection
Sep 22, 2022 · OAI

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 4, 2026 (checked Nov 8, 2026, unchanged)File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections9Nov 9, 2026Newest record Oct 28, 2026Current
Compliance actions1Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Sep 22, 2022San Diego, CADrugsOfficial Action Indicated (OAI)1000135880
Mar 12, 2018San Diego, CADrugsOfficial Action Indicated (OAI)1000135880
May 11, 2017San Diego, CADrugsVoluntary Action Indicated (VAI)1000135880
Nov 3, 2014San Diego, CADrugsVoluntary Action Indicated (VAI)1000135880
Jun 18, 2013San Diego, CADrugsVoluntary Action Indicated (VAI)1000135880
Feb 9, 2012San Diego, CADrugsNo Action Indicated (NAI)1000135880
Feb 2, 2011San Diego, CADrugsVoluntary Action Indicated (VAI)1000135880
Sep 1, 2010San Diego, CADrugsVoluntary Action Indicated (VAI)1000135880
Sep 11, 2009San Diego, CADrugsOfficial Action Indicated (OAI)1000135880

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 1000135880San Diego, CA9Sep 22, 2022

FDA data resources

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