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Belvas SA

FDA Regulatory Profile

Belvas SA has 0 FDA recalls, 2 inspections, 0 510(k) clearances and 0 compliance actions on record.

What these totals cover: FDA records filed under the name "Belvas SA" and its spelling variant "Belvas".

Latest inspection
Jan 21, 2019 · 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
Inspections2Nov 13, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

2 inspections from Jan 18, 2019 to Jan 21, 2019.

DateSiteProductClassificationFEI
Jan 21, 2019Duffel, BelgiumFood/CosmeticsNo Action Indicated (NAI)3014751037
Jan 18, 2019Ghislenghien, BelgiumFood/CosmeticsVoluntary Action Indicated (VAI)3010151362

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.

Look up the inspector observations behind these results with the FDA 483 search, or check for formal enforcement with the FDA warning letter search.

FDA-Inspected Facilities

2 inspected sites, newest inspection first.

FacilityLocationInspectionsLatest
FEI 3014751037Duffel, Belgium1Jan 21, 2019
FEI 3010151362Ghislenghien, Belgium1Jan 18, 2019

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FDA data resources

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