Transcity S.A.
FDA import alert and refusal historyGuayaquil, EcuadorFEI 3008809503
As of October 26, 2026, Transcity S.A. is not on any FDA import alert in SupplierRadar's records; FDA refused 12 of its shipment lines between February 21, 2018 and May 12, 2023, 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
- Mahi mahi · FILTHY
- Last warning letter
- None found
- Last inspection
- Classified VAI (Voluntary Action Indicated)
Every FDA record for Transcity S.A.
14 records, newest first. Each line links to the FDA page it came from.
2023
2018
2016
- InspectionInspection classified VAI (Voluntary Action Indicated)Foodborne Biological HazardsSource
2013
- InspectionInspection classified VAI (Voluntary Action Indicated)Foodborne Biological HazardsSource
Refusal charges, in plain English
- FILTHY12 refused lines
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.
- HISTAMINE2 refused lines
Histamine
The product appeared to contain histamine in a quantity that ordinarily makes it injurious to health.
Questions about Transcity S.A.
- Is Transcity S.A. on an FDA import alert?
- No listing for Transcity 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 Ecuador page.
- Has FDA refused shipments from Transcity S.A.?
- Yes. FDA refused 12 shipment lines from Transcity S.A. between February 21, 2018 and May 12, 2023. The most recent, on May 12, 2023, was mahi mahi, charged as FILTHY (filthy, putrid or decomposed substance).
- Why did FDA refuse Transcity S.A.'s shipments?
- The most frequent charges are FILTHY (filthy, putrid or decomposed substance, 12 lines) and HISTAMINE (histamine, 2 lines).
- When was Transcity S.A. last inspected by FDA?
- FDA's most recent inspection of Transcity S.A. with a final classification is dated November 18, 2016 and was classified VAI (Voluntary Action Indicated).
- What is Transcity S.A.'s FEI number?
- Transcity S.A.'s FDA Establishment Identifier (FEI) is 3008809503.
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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.