Dercher Enterprises, Inc.

FDA Regulatory Profile

Dercher Enterprises, Inc. has 0 FDA recalls, 6 inspections, 0 510(k) clearances and 1 compliance action on record.

Latest inspection
Sep 20, 2023 · OAI

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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
Inspections6Nov 8, 2026Newest record Oct 28, 2026Current
Compliance actions1Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Sep 20, 2023Upper Darby, PADrugsOfficial Action Indicated (OAI)2510734
Jun 13, 2022Upper Darby, PADrugsOfficial Action Indicated (OAI)2510734
May 4, 2021Upper Darby, PADrugsOfficial Action Indicated (OAI)2510734
Jan 19, 2017Upper Darby, PADrugsVoluntary Action Indicated (VAI)2510734
Jan 18, 2013Upper Darby, PADrugsVoluntary Action Indicated (VAI)2510734
Dec 18, 2008Upper Darby, PAFood/CosmeticsNo Action Indicated (NAI)2510734

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 2510734Upper Darby, PA6Sep 20, 2023

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