Newton Laboratories, Inc.

FDA Regulatory Profile

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

Latest inspection
Sep 17, 2021 · 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 9, 2026Newest record Oct 28, 2026Current
Compliance actions1Nov 2, 2026Newest record Oct 29, 2026Current

Recent FDA Inspections

DateSiteProductClassificationFEI
Sep 17, 2021Conyers, GADrugsVoluntary Action Indicated (VAI)1051203
Mar 30, 2018Conyers, GADrugsOfficial Action Indicated (OAI)1051203
Mar 29, 2017Conyers, GAVeterinaryVoluntary Action Indicated (VAI)1051203
Sep 29, 2015Conyers, GADrugsNo Action Indicated (NAI)1051203
Feb 18, 2015Conyers, GADrugsVoluntary Action Indicated (VAI)1051203
Jul 26, 2012Conyers, GADrugsVoluntary Action Indicated (VAI)1051203
Mar 11, 2010Conyers, GADrugsVoluntary Action Indicated (VAI)1051203

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 1051203Conyers, GA7Sep 17, 2021

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