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Degasa S.A. De C.V.

FDA Regulatory Profile

Degasa S.A. De C.V. has 0 FDA recalls, 2 inspections, 0 510(k) clearances and 1 compliance action on record.

Latest inspection
May 27, 2022 · OAI

Newer recall under related name Degasa Sa De Cv: Aug 4, 2017, D-1129-2017.

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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
Inspections2Nov 9, 2026Newest record Oct 28, 2026Current
Compliance actions1Nov 2, 2026Newest record Oct 29, 2026Current

Related names

NameRecalls510(k)InspectionsComplianceMost recent recall
Degasa Sa De Cv
Same company group		1000Aug 4, 2017 (D-1129-2017)

Recent FDA Inspections

DateSiteProductClassificationFEI
May 27, 2022Jiutepec, MexicoDrugsOfficial Action Indicated (OAI)3004555163
Sep 8, 2017Jiutepec, MexicoDrugsOfficial Action Indicated (OAI)3004555163

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 3004555163Jiutepec, Mexico2May 27, 2022

FDA data resources

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