RGH Enterprises Inc

FDA Regulatory Profile

RGH Enterprises Inc has 0 FDA recalls, 5 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Nov 4, 2025 · NAI

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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
Inspections5Nov 10, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Nov 4, 2025Jacksonville, FLFood/CosmeticsNo Action Indicated (NAI)3016677124
Aug 14, 2025Grove City, OHFood/CosmeticsNo Action Indicated (NAI)3025455941
Jul 26, 2024Fort Worth, TXFood/CosmeticsNo Action Indicated (NAI)3011198585
Mar 6, 2024Ontario, CAFood/CosmeticsNo Action Indicated (NAI)3011110317
Jan 19, 2016Halfmoon, NYFood/CosmeticsNo Action Indicated (NAI)3010183708

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 3016677124Jacksonville, FL1Nov 4, 2025
FEI 3025455941Grove City, OH1Aug 14, 2025
FEI 3011198585Fort Worth, TX1Jul 26, 2024
FEI 3011110317Ontario, CA1Mar 6, 2024
FEI 3010183708Halfmoon, NY1Jan 19, 2016

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