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Arkopharm Laboratories

FDA import alert and refusal historyCedex, FranceFEI 3004126919

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Example subjectArkopharm Laboratorie added to Import Alert 16-129 (red list)

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As of October 26, 2026, Arkopharm Laboratories is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on February 20, 2026, most often for product not listed with fda (NOT LISTED).

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

Current status

Import alerts
Not listed
Last import refusal
Vitamin, n.e.c. · NOT LISTED
Last warning letter
None found
Last inspection
None on record

Every FDA record for Arkopharm Laboratories

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

2026

  1. Import refusal
    Refused, Vitamin, n.e.c.NOT LISTEDUNAPPROVEDEntry 799-2883527-7
    Source

Refusal charges, in plain English

  • NOT LISTED1 refused line

    Product not listed with FDA

    The product appeared to be a drug or device that is not included in the listing FDA requires under section 510(j) of the FD&C Act.

  • UNAPPROVED1 refused line

    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 Arkopharm Laboratories

Is Arkopharm Laboratories on an FDA import alert?
No listing for Arkopharm Laboratories appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the France page.
Has FDA refused shipments from Arkopharm Laboratories?
Yes. FDA refused 1 shipment line from Arkopharm Laboratories on February 20, 2026. The most recent, on February 20, 2026, was vitamin, n.e.c., charged as NOT LISTED (product not listed with fda).
Why did FDA refuse Arkopharm Laboratories's shipments?
The most frequent charges are NOT LISTED (product not listed with fda, 1 line) and UNAPPROVED (unapproved new drug, 1 line).
What is Arkopharm Laboratories's FEI number?
Arkopharm Laboratories's FDA Establishment Identifier (FEI) is 3004126919.

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Example subjectArkopharm Laboratorie 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.