SupplierRadar

Templanza S.A. de C.V.

FDA import alert and refusal historyLa Libertad, El SalvadorFEI 3012541634

Recorded by FDA as TEMPLANZA S.A. DE C.V.

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Example subjectTemplanza S.A. de C.V added to Import Alert 16-129 (red list)

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As of October 26, 2026, Templanza S.A. de C.V. is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on January 11, 2017, most often for filthy, putrid or decomposed substance (FILTHY).

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

Current status

Import alerts
Not listed
Last import refusal
Tortillas · FILTHY
Last warning letter
None found
Last inspection
None on record

Every FDA record for Templanza S.A. de C.V.

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

2017

  1. Import refusal
    Refused, TortillasFILTHYEntry U42-0050907-1
    Source

Refusal charges, in plain English

  • FILTHY1 refused line

    Filthy, putrid or decomposed substance

    The product appeared to consist in whole or in part of a filthy, putrid, or decomposed substance, or to be otherwise unfit for food.

Questions about Templanza S.A. de C.V.

Is Templanza S.A. de C.V. on an FDA import alert?
No listing for Templanza S.A. de C.V. appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the El Salvador page.
Has FDA refused shipments from Templanza S.A. de C.V.?
Yes. FDA refused 1 shipment line from Templanza S.A. de C.V. on January 11, 2017. The most recent, on January 11, 2017, was tortillas, charged as FILTHY (filthy, putrid or decomposed substance).
Why did FDA refuse Templanza S.A. de C.V.'s shipments?
The most frequent charge is FILTHY (filthy, putrid or decomposed substance, 1 line).
What is Templanza S.A. de C.V.'s FEI number?
Templanza S.A. de C.V.'s FDA Establishment Identifier (FEI) is 3012541634.

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Example subjectTemplanza S.A. de C.V 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.