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Bayer de Mexico, S.A. de C.V.

FDA import alert and refusal historyLerma, MexicoFEI 3002806479

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

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As of October 26, 2026, Bayer de Mexico, S.A. de C.V. is not on any FDA import alert in SupplierRadar's records; FDA refused 6 of its shipment lines between June 28, 2019 and October 8, 2026, 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 c (ascorbic acid) · UNAPPROVED
Last warning letter
None found
Last inspection
None on record

Every FDA record for Bayer de Mexico, S.A. de C.V.

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

2026

  1. Import refusal
    Refused, Vitamin c (ascorbic acid)UNAPPROVEDEntry AEK-9843471-3
    Source

2024

  1. Import refusal
    Refused, Vitamin c (ascorbic acid)UNAPPROVEDEntry AEK-5502822-7
    Source

2022

  1. Import refusal
    Refused, L-carnitine (protein)NEW VET DREntry 799-0673037-9
    Source

2021

  1. Import refusal
    Refused, Vitamin b1 (thiamine)UNAPPROVEDEntry 799-2329327-7
    Source

2019

  1. Import refusal
    Refused, 2 lines in one entry: Multiple vitamins (mvi-12 vitamin combo) (vitamin); Vitamin b12 (cyanocobalamin)UNAPPROVEDEntry 799-1601440-8Show 2 lines
    Source

Refusal charges, in plain English

  • UNAPPROVED5 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.

  • NEW VET DR1 refused line

    NEW VET DR

Questions about Bayer de Mexico, S.A. de C.V.

Is Bayer de Mexico, S.A. de C.V. on an FDA import alert?
No listing for Bayer de Mexico, 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 Bayer de Mexico, S.A. de C.V.?
Yes. FDA refused 6 shipment lines from Bayer de Mexico, S.A. de C.V. between June 28, 2019 and October 8, 2026. The most recent, on October 8, 2026, was vitamin c (ascorbic acid), charged as UNAPPROVED (unapproved new drug).
Why did FDA refuse Bayer de Mexico, S.A. de C.V.'s shipments?
The most frequent charges are UNAPPROVED (unapproved new drug, 5 lines) and NEW VET DR (new vet dr, 1 line).
What is Bayer de Mexico, S.A. de C.V.'s FEI number?
Bayer de Mexico, S.A. de C.V.'s FDA Establishment Identifier (FEI) is 3002806479.

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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.