Atlantic Management Resources Ltd.

FDA Regulatory Profile

Atlantic Management Resources Ltd. has 5 FDA recalls, 1 inspection, 0 510(k) clearances and 1 compliance action on record.

Latest recall
D-0629-2025 · Class II · Aug 27, 2025
Latest inspection
Aug 10, 2022 · OAI

Reviewing Atlantic Management Resources Ltd. as a supplier? Request a free FDA snapshot: name up to five suppliers and get a PDF of their public FDA record, with sources and dates. You do not need an API connection. Each snapshot is prepared by hand.

Check this supplier

Or check Atlantic Management Resources Ltd. yourself in Claude, Cursor or ChatGPT: get the full FDA risk summary, with inspections, warning letters, Form 483s and import alerts by site.

Get a free API key

Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls5Nov 4, 2026 (checked Nov 8, 2026, unchanged)File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections1Nov 9, 2026Newest record Oct 28, 2026Current
Compliance actions1Nov 2, 2026Newest record Oct 29, 2026Current

Recent Recalls

NumberClassProductDate
D-0629-2025Class IINeuroquell & Neuroquell Plus, .22 fl. Oz (6.6mL),Mfg. For/Dist. By Claire Ellen Products, P.O. Box…Aug 27, 2025
D-0083-2023Class IIProSirona, A Homeopathic Formula, Calendula Oil packaged in 1/8 Fl. oz. (3.5 g) bottles, Dist. by…Dec 12, 2022
D-0084-2023Class IIMenastil, A Homeopathic Formula, Calendula Oil packaged in 1/8 Fl. oz. (3.5 g) bottles, Mfg…Dec 12, 2022
D-0082-2023Class IINeuroquell, A Homeopathic Drug, Calendula Oil, packaged in1/8 Fl. oz. (3.5 g) bottles, Mfg…Dec 12, 2022
D-0081-2023Class IINeuroquell Plus, Advanced Formula, A Homeopathic Drug, Calendula Oil packaged in 0.22 Fl. oz. (6.6…Dec 12, 2022

Recent FDA Inspections

DateSiteProductClassificationFEI
Aug 10, 2022Westborough, MADrugsOfficial Action Indicated (OAI)3014117482

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 3014117482Westborough, MA1Aug 10, 2022

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