SupplierRadar

Laboratorios Grossman SA de V

FDA import alert and refusal historyDeleg Coyoacan, MexicoFEI 3027591660

Recorded by FDA as LABORATORIOS GROSSMAN SA DE V

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Example subjectLaboratorios Grossman SA de added to Import Alert 16-129 (red list)

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As of October 26, 2026, Laboratorios Grossman SA de V is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines between July 16, 2024 and August 13, 2025, 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
Hydroxocobalamin (vitamin) · UNAPPROVED
Last warning letter
None found
Last inspection
None on record

Every FDA record for Laboratorios Grossman SA de V

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

2025

  1. Import refusal
    Refused, Hydroxocobalamin (vitamin)UNAPPROVEDEntry 799-9455196-9
    Source

2024

  1. Import refusal
    Refused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.UNAPPROVEDEntry 799-1456347-4
    Source

Refusal charges, in plain English

  • UNAPPROVED2 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 Laboratorios Grossman SA de V

Is Laboratorios Grossman SA de V on an FDA import alert?
No listing for Laboratorios Grossman SA de 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 Laboratorios Grossman SA de V?
Yes. FDA refused 2 shipment lines from Laboratorios Grossman SA de V between July 16, 2024 and August 13, 2025. The most recent, on August 13, 2025, was hydroxocobalamin (vitamin), charged as UNAPPROVED (unapproved new drug).
Why did FDA refuse Laboratorios Grossman SA de V's shipments?
The most frequent charge is UNAPPROVED (unapproved new drug, 2 lines).
What is Laboratorios Grossman SA de V's FEI number?
Laboratorios Grossman SA de V's FDA Establishment Identifier (FEI) is 3027591660.

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Example subjectLaboratorios Grossman SA de 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.