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Laboratorio Lamfer

FDA import alert and refusal historySacatepequez, GuatemalaFEI 3011410158

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Example subjectLaboratorio Lamfe added to Import Alert 16-129 (red list)

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As of October 25, 2026, Laboratorio Lamfer is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines on September 24, 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
Zinc (mineral) · UNAPPROVED
Last warning letter
None found
Last inspection
None on record

Every FDA record for Laboratorio Lamfer

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

2025

  1. Import refusal
    Refused, 2 lines in one entry: Zinc (mineral); Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.UNAPPROVEDEntry AEK-7567983-5Show 2 lines
    • Refused, Zinc (mineral)UNAPPROVEDEntry AEK-7567983-5Source
    • Refused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.UNAPPROVEDEntry AEK-7567983-5Source
    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 Laboratorio Lamfer

Is Laboratorio Lamfer on an FDA import alert?
No listing for Laboratorio Lamfer appears in the FDA import alerts SupplierRadar checked on October 25, 2026. Country-wide alerts may still apply to its products; see the Guatemala page.
Has FDA refused shipments from Laboratorio Lamfer?
Yes. FDA refused 2 shipment lines from Laboratorio Lamfer on September 24, 2025. The most recent, on September 24, 2025, was zinc (mineral), charged as UNAPPROVED (unapproved new drug).
Why did FDA refuse Laboratorio Lamfer's shipments?
The most frequent charge is UNAPPROVED (unapproved new drug, 2 lines).
What is Laboratorio Lamfer's FEI number?
Laboratorio Lamfer's FDA Establishment Identifier (FEI) is 3011410158.

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Example subjectLaboratorio Lamfe 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.