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Productos Medix, S.A. de C.V.

FDA import alert and refusal historyMexico Df, MexicoFEI 3009932533

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Example subjectProductos Medix, S.A. de C.V added to Import Alert 16-129 (red list)

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As of October 26, 2026, Productos Medix, S.A. de C.V. is not on any FDA import alert in SupplierRadar's records; FDA refused 3 of its shipment lines between February 1, 2021 and July 20, 2023, 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 d2 (calciferol) · UNAPPROVED
Last warning letter
None found
Last inspection
None on record

Every FDA record for Productos Medix, S.A. de C.V.

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

2023

  1. Import refusal
    Refused, Vitamin d2 (calciferol)UNAPPROVEDEntry AEK-3609788-7
    Source

2022

  1. Import refusal
    Refused, Vitamin, n.e.c.UNAPPROVEDEntry SCS-1848968-5
    Source

2021

  1. Import refusal
    Refused, Vitamin d2 (calciferol)UNAPPROVEDEntry 799-0249463-1
    Source

Refusal charges, in plain English

  • UNAPPROVED3 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 Productos Medix, S.A. de C.V.

Is Productos Medix, S.A. de C.V. on an FDA import alert?
No listing for Productos Medix, S.A. de C.V. appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Mexico page.
Has FDA refused shipments from Productos Medix, S.A. de C.V.?
Yes. FDA refused 3 shipment lines from Productos Medix, S.A. de C.V. between February 1, 2021 and July 20, 2023. The most recent, on July 20, 2023, was vitamin d2 (calciferol), charged as UNAPPROVED (unapproved new drug).
Why did FDA refuse Productos Medix, S.A. de C.V.'s shipments?
The most frequent charge is UNAPPROVED (unapproved new drug, 3 lines).
What is Productos Medix, S.A. de C.V.'s FEI number?
Productos Medix, S.A. de C.V.'s FDA Establishment Identifier (FEI) is 3009932533.

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Example subjectProductos Medix, S.A. de C.V 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.