SupplierRadar

Iak

FDA import alert and refusal historyGuatemala, GuatemalaFEI 3013723557

Recorded by FDA as IAK

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

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As of October 25, 2026, Iak is not on any FDA import alert in SupplierRadar's records; FDA refused 3 of its shipment lines between August 28, 2020 and December 31, 2024, most often for required label information not in english (NO ENGLISH).

Data from FDA public records, last checked . Request a correction

Current status

Import alerts
Not listed
Last import refusal
Apple, core fruit juices or concentrates · NO ENGLISH
Last warning letter
None found
Last inspection
None on record

Every FDA record for Iak

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

2024

  1. Import refusal
    Refused, 2 lines in one entry: Apple, core fruit juices or concentratesNO ENGLISHEntry E84-0116787-7Show 2 lines
    • Refused, Apple, core fruit juices or concentratesNO ENGLISHEntry E84-0116787-7Source
    • Refused, Apple, core fruit juices or concentratesNO ENGLISHEntry E84-0116787-7Source
    Source

2020

  1. Import refusal
    Refused, Beverage base, pit fruit, liquidNO ENGLISHEntry H35-2038302-3
    Source

Refusal charges, in plain English

  • NO ENGLISH3 refused lines

    Required label information not in English

    Information that must appear on the label appeared not to be given in English, or not to be repeated in every language used on the label.

Questions about Iak

Is Iak on an FDA import alert?
No listing for Iak 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 Iak?
Yes. FDA refused 3 shipment lines from Iak between August 28, 2020 and December 31, 2024. The most recent, on December 31, 2024, was apple, core fruit juices or concentrates, charged as NO ENGLISH (required label information not in english).
Why did FDA refuse Iak's shipments?
The most frequent charge is NO ENGLISH (required label information not in english, 3 lines).
What is Iak's FEI number?
Iak's FDA Establishment Identifier (FEI) is 3013723557.

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Example subjectIa 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.