DSC Laboratories, Inc.

FDA Regulatory Profile

DSC Laboratories, Inc. has 0 FDA recalls, 7 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Jul 16, 2025 · VAI

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

Recent FDA Inspections

DateSiteProductClassificationFEI
Jul 16, 2025Muskegon, MIDrugsVoluntary Action Indicated (VAI)1831691
Oct 11, 2017Muskegon, MIDrugsVoluntary Action Indicated (VAI)1831691
Aug 25, 2015Muskegon, MIDrugsVoluntary Action Indicated (VAI)1831691
Aug 31, 2012Muskegon, MIDrugsVoluntary Action Indicated (VAI)1831691
Jun 27, 2011Muskegon, MIDrugsVoluntary Action Indicated (VAI)1831691
Apr 13, 2010Muskegon, MIDrugsVoluntary Action Indicated (VAI)1831691
Jul 17, 2009Muskegon, MIDrugsNo Action Indicated (NAI)1831691

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 1831691Muskegon, MI7Jul 16, 2025

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