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PRODEMAN S.A.

FDA Regulatory Profile

PRODEMAN S.A. has 0 FDA recalls, 1 inspection, 0 510(k) clearances and 0 compliance actions on record.

What these totals cover: FDA records filed under the name "PRODEMAN S.A." and its spelling variant "Prodeman".

Latest inspection
Dec 18, 2015 · VAI

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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
Inspections1Nov 13, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

1 inspection on Dec 18, 2015.

DateSiteProductClassificationFEI
Dec 18, 2015General Cabrera, ArgentinaFood/CosmeticsVoluntary Action Indicated (VAI)3013765314

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

1 inspected site, newest inspection first.

FacilityLocationInspectionsLatest
FEI 3013765314General Cabrera, Argentina1Dec 18, 2015

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FDA data resources

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