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COMUMAP S.A

FDA Regulatory Profile

COMUMAP S.A 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 "COMUMAP S.A" and its spelling variant "Comumap".

Latest inspection
Nov 10, 2016 · 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
Inspections2Nov 13, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

2 inspections from Apr 12, 2013 to Nov 10, 2016.

DateSiteProductClassificationFEI
Nov 10, 2016Chanduy, EcuadorFood/CosmeticsVoluntary Action Indicated (VAI)3013267585
Apr 12, 2013Chanduy, EcuadorFood/CosmeticsNo Action Indicated (NAI)3013267585

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 3013267585Chanduy, Ecuador2Nov 10, 2016

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FDA data resources

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