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Lab Lafage

FDA import alert and refusal historyBofasa, GuatemalaFEI 3043016810

Recorded by FDA as LAB LAFAGE

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Example subjectLab Lafag added to Import Alert 16-129 (red list)

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As of October 26, 2026, Lab Lafage is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on September 25, 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 e (tocopherol) · UNAPPROVED
Last warning letter
None found
Last inspection
None on record

Every FDA record for Lab Lafage

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

2026

  1. Import refusal
    Refused, Vitamin e (tocopherol)UNAPPROVEDEntry 1FX-4166735-4
    Source

Refusal charges, in plain English

  • 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 Lab Lafage

Is Lab Lafage on an FDA import alert?
No listing for Lab Lafage appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Guatemala page.
Has FDA refused shipments from Lab Lafage?
Yes. FDA refused 1 shipment line from Lab Lafage on September 25, 2026. The most recent, on September 25, 2026, was vitamin e (tocopherol), charged as UNAPPROVED (unapproved new drug).
Why did FDA refuse Lab Lafage's shipments?
The most frequent charge is UNAPPROVED (unapproved new drug, 1 line).
What is Lab Lafage's FEI number?
Lab Lafage's FDA Establishment Identifier (FEI) is 3043016810.

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Example subjectLab Lafag 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.