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The Richline Group Inc

FDA Regulatory Profile

The Richline Group Inc has 0 FDA recalls, 4 inspections, 0 510(k) clearances and 1 compliance action on record.

Latest inspection
Apr 16, 2025 · 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
Inspections4Nov 8, 2026Newest record Oct 28, 2026Current
Compliance actions1Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Apr 16, 2025Tamarac, FLDevicesOfficial Action Indicated (OAI)3006749547
Jan 12, 2024Tamarac, FLDevicesOfficial Action Indicated (OAI)3006749547
Nov 3, 2016Tamarac, FLDrugsVoluntary Action Indicated (VAI)3006749547
Nov 25, 2014Attleboro, MADrugsNo Action Indicated (NAI)2243569

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 3006749547Tamarac, FL3Apr 16, 2025
FEI 2243569Attleboro, MA1Nov 25, 2014

FDA data resources

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