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Integrated Commercialization Solutions LLC

FDA Regulatory Profile

Integrated Commercialization Solutions LLC has 0 FDA recalls, 13 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Sep 23, 2025 · NAI

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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
Inspections13Nov 10, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Sep 23, 2025Reno, NVDrugsNo Action Indicated (NAI)3011851024
Aug 8, 2025Brooks, KYDrugsNo Action Indicated (NAI)3002478693
May 15, 2025Lockbourne, OHDrugsVoluntary Action Indicated (VAI)3014408462
Jul 15, 2019Brooks, KYDrugsVoluntary Action Indicated (VAI)3002478693
Sep 13, 2018Lockbourne, OHDrugsNo Action Indicated (NAI)3014408462
Jan 18, 2018Reno, NVDrugsVoluntary Action Indicated (VAI)3011851024
Dec 12, 2013Brooks, KYDrugsNo Action Indicated (NAI)3002478693
Mar 28, 2012Brooks, KYDrugsNo Action Indicated (NAI)3002478693
Jan 3, 2011Brooks, KYDrugsOfficial Action Indicated (OAI)3002478693
Oct 7, 2010Brooks, KYDrugsNo Action Indicated (NAI)3002478693
Jun 24, 2010Brooks, KYDrugsNo Action Indicated (NAI)3002478693
Feb 5, 2010Brooks, KYDrugsNo Action Indicated (NAI)3002478693
Jan 6, 2010Reno, NVBiologicsNo Action Indicated (NAI)3011851024

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 3011851024Reno, NV3Sep 23, 2025
FEI 3002478693Brooks, KY8Aug 8, 2025
FEI 3014408462Lockbourne, OH2May 15, 2025

FDA data resources

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