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Lanketin

FDA import alert and refusal historyGuatemala, GuatemalaFEI 3040055810

Recorded by FDA as LANKETIN

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

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As of October 26, 2026, Lanketin is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines between October 22, 2025 and December 2, 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
Vitamin, n.e.c. · UNAPPROVED
Last warning letter
None found
Last inspection
None on record

Every FDA record for Lanketin

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

2025

  1. Import refusal
    Refused, Vitamin, n.e.c.UNAPPROVEDEntry 799-8413405-8
    Source
  2. Import refusal
    Refused, Multiple vitamins (mvi-12 vitamin combo) (vitamin)UNAPPROVEDEntry 799-4187016-6
    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 Lanketin

Is Lanketin on an FDA import alert?
No listing for Lanketin 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 Lanketin?
Yes. FDA refused 2 shipment lines from Lanketin between October 22, 2025 and December 2, 2025. The most recent, on December 2, 2025, was vitamin, n.e.c., charged as UNAPPROVED (unapproved new drug).
Why did FDA refuse Lanketin's shipments?
The most frequent charge is UNAPPROVED (unapproved new drug, 2 lines).
What is Lanketin's FEI number?
Lanketin's FDA Establishment Identifier (FEI) is 3040055810.

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Example subjectLanketi 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.