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Talisman Limited

FDA Regulatory Profile

Talisman Limited has 0 FDA recalls, 4 inspections, 0 510(k) clearances and 3 compliance actions on record.

Latest inspection
Jan 31, 2024 · VAI

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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
Inspections4Nov 8, 2026Newest record Oct 28, 2026Current
Compliance actions3Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Jan 31, 2024Richardson, TXFood/CosmeticsVoluntary Action Indicated (VAI)3011235018
May 30, 2013Leesburg, VADevicesNo Action Indicated (NAI)3004585612
Nov 18, 2010Leesburg, VADevicesNo Action Indicated (NAI)3004585612
Nov 12, 2009Leesburg, VADevicesOfficial Action Indicated (OAI)3004585612

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 3011235018Richardson, TX1Jan 31, 2024
FEI 3004585612Leesburg, VA3May 30, 2013

FDA data resources

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