Agropharma Laboratories Inc.

FDA Regulatory Profile

Agropharma Laboratories Inc. has 0 FDA recalls, 7 inspections, 0 510(k) clearances and 1 compliance action on record.

Latest inspection
Nov 3, 2021 · 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
Inspections7Nov 9, 2026Newest record Oct 28, 2026Current
Compliance actions1Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Nov 3, 2021Salinas, PRDrugsOfficial Action Indicated (OAI)3000203462
Sep 14, 2018Salinas, PRDrugsVoluntary Action Indicated (VAI)3000203462
Feb 12, 2016Salinas, PRVeterinaryVoluntary Action Indicated (VAI)3000203462
Mar 20, 2013Salinas, PRVeterinaryVoluntary Action Indicated (VAI)3000203462
Jul 19, 2011Salinas, PRFood/CosmeticsVoluntary Action Indicated (VAI)3000203462
May 7, 2010Salinas, PRDrugsVoluntary Action Indicated (VAI)3000203462
Aug 19, 2009Salinas, PRDrugsVoluntary Action Indicated (VAI)3000203462

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 3000203462Salinas, PR7Nov 3, 2021

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