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Advanced Orthomolecular Research Inc

FDA import alert and refusal historyCalgary, CanadaFEI 3010118561

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Example subjectAdvanced Orthomolecular Research In added to Import Alert 16-129 (red list)

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As of October 26, 2026, Advanced Orthomolecular Research Inc is not on any FDA import alert in SupplierRadar's records; FDA refused 10 of its shipment lines between February 27, 2018 and February 4, 2021, most often for unapproved new drug (UNAPPROVED).

Data from FDA public records, last checked . Request a correction

Current status

Import alerts
Not listed
Last import refusal
Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c. · UNAPPROVED
Last warning letter
None found
Last inspection
None on record

Every FDA record for Advanced Orthomolecular Research Inc

10 records, newest first. Each line links to the FDA page it came from.

2021

  1. Import refusal
    Refused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.UNAPPROVEDEntry 9R3-0010157-5
    Source
  2. Import refusal
    Refused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.UNAPPROVEDEntry 9R3-0010156-7
    Source
  3. Import refusal
    Refused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.UNAPPROVEDEntry AEK-8590682-1
    Source

2020

  1. Import refusal
    Refused, 6 lines in one entry: Vitamin e (tocopherol); Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.UNAPPROVEDEntry AEK-7870081-9Show 6 lines
    • Refused, Vitamin e (tocopherol)UNAPPROVEDEntry AEK-7870081-9Source
    • Refused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.UNAPPROVEDEntry AEK-7870081-9Source
    • Refused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.UNAPPROVEDEntry AEK-7870081-9Source
    • Refused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.UNAPPROVEDEntry AEK-7870081-9Source
    • Refused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.UNAPPROVEDEntry AEK-7870081-9Source
    • Refused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.UNAPPROVEDEntry AEK-7870081-9Source
    Source

2018

  1. Import refusal
    Refused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.UNAPPROVEDEntry 300-2545773-0
    Source

Refusal charges, in plain English

  • UNAPPROVED10 refused lines

    Unapproved new drug

    The product appeared to be a new drug within the meaning of section 201(p) of the FD&C Act without an approved New Drug Application. FDA can apply this charge to a food or supplement whose labeling presents it for drug uses.

Questions about Advanced Orthomolecular Research Inc

Is Advanced Orthomolecular Research Inc on an FDA import alert?
No listing for Advanced Orthomolecular Research Inc appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Canada page.
Has FDA refused shipments from Advanced Orthomolecular Research Inc?
Yes. FDA refused 10 shipment lines from Advanced Orthomolecular Research Inc between February 27, 2018 and February 4, 2021. The most recent, on February 4, 2021, was vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c., charged as UNAPPROVED (unapproved new drug).
Why did FDA refuse Advanced Orthomolecular Research Inc's shipments?
The most frequent charge is UNAPPROVED (unapproved new drug, 10 lines).
What is Advanced Orthomolecular Research Inc's FEI number?
Advanced Orthomolecular Research Inc's FDA Establishment Identifier (FEI) is 3010118561.

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Example subjectAdvanced Orthomolecular Research In added to Import Alert 16-129 (red list)

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SupplierRadar is not affiliated with the U.S. Food and Drug Administration. Data comes from public FDA records and may contain errors. This is not legal advice; importers remain responsible for their supplier evaluations.