BHC, LLC

FDA Regulatory Profile

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

Latest inspection
Aug 11, 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
Inspections4Nov 10, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Aug 11, 2025Brownsburg, INBiologicsNo Action Indicated (NAI)3009651519
Jun 30, 2023Brownsburg, INBiologicsVoluntary Action Indicated (VAI)3009651519
Apr 26, 2018Brownsburg, INBiologicsNo Action Indicated (NAI)3009651519
Jan 27, 2016Brownsburg, INBiologicsNo Action Indicated (NAI)3009651519

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 3009651519Brownsburg, IN4Aug 11, 2025

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