Cat Tien Co., Ltd
FDA import alert and refusal historyNha Trang, VietnamFEI 3012910098
As of October 26, 2026, Cat Tien Co., Ltd (Nha Trang, Vietnam) is on the red list of FDA Import Alert 16-105 (Fish products: decomposition, histamine or indole) for mahi mahi, published by FDA on April 1, 2022, and has 9 FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 16-105 · red list
- Last import refusal
- Mahi mahi · FILTHY
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Cat Tien Co., Ltd
10 records, newest first. Each line links to the FDA page it came from.
2022
- Import alert listingListed on Import Alert 16-105red listMahi MahiSource
2018
2017
Refusal charges, in plain English
- FILTHY9 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.
Questions about Cat Tien Co., Ltd
- Is Cat Tien Co., Ltd on an FDA import alert?
- Yes. As of October 26, 2026, Cat Tien Co., Ltd is on the red list of FDA Import Alert 16-105, “Fish products: decomposition, histamine or indole”, for mahi mahi; FDA published the listing on April 1, 2022.
- Has FDA refused shipments from Cat Tien Co., Ltd?
- Yes. FDA refused 9 shipment lines from Cat Tien Co., Ltd between August 18, 2017 and June 26, 2018. The most recent, on June 26, 2018, was mahi mahi, charged as FILTHY (filthy, putrid or decomposed substance).
- Why did FDA refuse Cat Tien Co., Ltd's shipments?
- The most frequent charge is FILTHY (filthy, putrid or decomposed substance, 9 lines).
- What is Cat Tien Co., Ltd's FEI number?
- Cat Tien Co., Ltd's FDA Establishment Identifier (FEI) is 3012910098.
- Can shipments from Cat Tien Co., Ltd still enter the U.S.?
- Shipments of mahi mahi from Cat Tien Co., Ltd can be detained without physical examination under Import Alert 16-105; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).
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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.