SupplierRadar

Triguisar de Colombia S.A

FDA import alert and refusal historyItagui, ColombiaFEI 3004325432

Recorded by FDA as TRIGUISAR DE COLOMBIA S.A

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Example subjectTriguisar de Colombia S. added to Import Alert 16-129 (red list)

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As of October 26, 2026, Triguisar de Colombia S.A is not on any FDA import alert in SupplierRadar's records; FDA refused 4 of its shipment lines between August 1, 2018 and February 3, 2023, 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
Mixed spices and seasonings, liquid, without salt, n.e.c. · LACKS FIRM
Last warning letter
None found
Last inspection
Classified VAI (Voluntary Action Indicated)

Every FDA record for Triguisar de Colombia S.A

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

2023

  1. Import refusal
    Refused, Mixed spices and seasonings, liquid, without salt, n.e.c.LACKS FIRMLACKS N/CNO ENGLISHCOLORLABELEntry AMN-0082578-2
    Source

2022

  1. Import refusal
    Refused, Mixed spices and seasonings, liquid, without salt, n.e.c.UNSAFE COLEntry AMN-0068577-2
    Source

2019

  1. Import refusal
    Refused, Whole spice, n.e.c.NO ENGLISHEntry B4Y-0009981-4
    Source
  2. Inspection
    Inspection classified VAI (Voluntary Action Indicated)Foodborne Biological Hazards
    Source

2018

  1. Import refusal
    Refused, Mixed spice and seasonings, ground, cracked, without salt, n.e.c.NO ENGLISHEntry AMN-0040672-4
    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.

  • COLORLABEL1 refused line

    Required information not prominent

    Information required on the label appeared not to be placed prominently enough, or in such terms, to be read and understood by an ordinary consumer.

  • LACKS FIRM1 refused line

    Manufacturer name and address missing

    The packaged product's label appeared not to show the name and place of business of the manufacturer, packer, or distributor.

  • LACKS N/C1 refused line

    Net quantity statement missing

    The packaged food appeared not to carry an accurate statement of the quantity of contents, such as net weight, measure, or count, on its label.

  • UNSAFE COL1 refused line

    Color additive unsafe under section 721

    The product appeared to be, or to contain, a color additive that is unsafe within the meaning of section 721(a) of the FD&C Act, the section that governs which color additives may be used and how.

Questions about Triguisar de Colombia S.A

Is Triguisar de Colombia S.A on an FDA import alert?
No listing for Triguisar de Colombia S.A appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Colombia page.
Has FDA refused shipments from Triguisar de Colombia S.A?
Yes. FDA refused 4 shipment lines from Triguisar de Colombia S.A between August 1, 2018 and February 3, 2023. The most recent, on February 3, 2023, was mixed spices and seasonings, liquid, without salt, n.e.c., charged as LACKS FIRM (manufacturer name and address missing).
Why did FDA refuse Triguisar de Colombia S.A's shipments?
The most frequent charges are NO ENGLISH (required label information not in english, 3 lines) and COLORLABEL (required information not prominent, 1 line).
When was Triguisar de Colombia S.A last inspected by FDA?
FDA's most recent inspection of Triguisar de Colombia S.A with a final classification is dated April 4, 2019 and was classified VAI (Voluntary Action Indicated).
What is Triguisar de Colombia S.A's FEI number?
Triguisar de Colombia S.A's FDA Establishment Identifier (FEI) is 3004325432.

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Example subjectTriguisar de Colombia S. 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.