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Continental Services Group, Inc.

FDA Regulatory Profile

Continental Services Group, Inc. has 0 FDA recalls, 11 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Jul 24, 2024 · 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
Inspections11Nov 9, 2026Newest record Oct 28, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Jul 24, 2024Ft Lauderdale, FLBiologicsVoluntary Action Indicated (VAI)1047134
May 21, 2024Miami, FLBiologicsVoluntary Action Indicated (VAI)1070217
Aug 24, 2022Ft Lauderdale, FLBiologicsNo Action Indicated (NAI)1047134
Aug 24, 2022Miami, FLBiologicsVoluntary Action Indicated (VAI)1070217
Jul 9, 2019Miami, FLBiologicsVoluntary Action Indicated (VAI)1070217
May 31, 2019Ft Lauderdale, FLBiologicsVoluntary Action Indicated (VAI)1047134
Aug 22, 2017Miami, FLBiologicsVoluntary Action Indicated (VAI)1070217
Oct 1, 2014Ft Lauderdale, FLBiologicsVoluntary Action Indicated (VAI)1047134
Sep 27, 2013Ft Lauderdale, FLBiologicsVoluntary Action Indicated (VAI)1047134
Jul 14, 2011Ft Lauderdale, FLBiologicsVoluntary Action Indicated (VAI)1047134
Jan 14, 2009Ft Lauderdale, FLBiologicsNo Action Indicated (NAI)1047134

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 1047134Ft Lauderdale, FL7Jul 24, 2024
FEI 1070217Miami, FL4May 21, 2024

FDA data resources

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