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Andapharm, LLC

FDA Regulatory Profile

Andapharm, LLC has 0 FDA recalls, 4 inspections, 0 510(k) clearances and 2 compliance actions on record.

Latest inspection
Jul 18, 2018 · 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
Inspections4Nov 9, 2026Newest record Oct 28, 2026Current
Compliance actions2Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Jul 18, 2018Fort Lauderdale, FLDrugsOfficial Action Indicated (OAI)3005000348
Feb 26, 2016Fort Lauderdale, FLDrugsVoluntary Action Indicated (VAI)3005000348
Feb 7, 2012Fort Lauderdale, FLDrugsVoluntary Action Indicated (VAI)3005000348
Aug 7, 2009Fort Lauderdale, FLDrugsVoluntary Action Indicated (VAI)3005000348

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 3005000348Fort Lauderdale, FL4Jul 18, 2018

FDA data resources

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