SupplierRadar

Pharma Medico ApS

FDA import alert and refusal historyAarhus C, DenmarkFEI 2000031304

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Example subjectPharma Medico Ap added to Import Alert 16-129 (red list)

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As of October 26, 2026, Pharma Medico ApS is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on January 18, 2017, most often for no u.s. adverse event contact on supplement label (NCONTACT).

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

Current status

Import alerts
Not listed
Last import refusal
Herbals & botanicals (not teas), n.e.c. · NCONTACT
Last warning letter
None found
Last inspection
None on record

Every FDA record for Pharma Medico ApS

1 record, newest first. Each line links to the FDA page it came from.

2017

  1. Import refusal
    Refused, Herbals & botanicals (not teas), n.e.c.NCONTACTEntry AEK-2870398-8
    Source

Refusal charges, in plain English

  • NCONTACT1 refused line

    No U.S. adverse event contact on supplement label

    The dietary supplement label appeared not to show a U.S. address or phone number through which a serious adverse event can be reported.

Questions about Pharma Medico ApS

Is Pharma Medico ApS on an FDA import alert?
No listing for Pharma Medico ApS appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Denmark page.
Has FDA refused shipments from Pharma Medico ApS?
Yes. FDA refused 1 shipment line from Pharma Medico ApS on January 18, 2017. The most recent, on January 18, 2017, was herbals & botanicals (not teas), n.e.c., charged as NCONTACT (no u.s. adverse event contact on supplement label).
Why did FDA refuse Pharma Medico ApS's shipments?
The most frequent charge is NCONTACT (no u.s. adverse event contact on supplement label, 1 line).
What is Pharma Medico ApS's FEI number?
Pharma Medico ApS's FDA Establishment Identifier (FEI) is 2000031304.

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Example subjectPharma Medico Ap 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.