GGC TWN. Co., Ltd.
FDA import alert and refusal historyAmphur Mueang Phuket, ThailandFEI 3004264815
As of October 26, 2026, GGC TWN. Co., Ltd. (Amphur Mueang Phuket, Thailand) is on the red list of FDA Import Alert 16-105 (Fish products: decomposition, histamine or indole) for tuna, published by FDA on February 1, 2019, and has 14 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
- Tuna (albacore, yellowfin, bluefin, skipjack, etc.) · HISTAMINE
- Last warning letter
- None found
- Last inspection
- Classified VAI (Voluntary Action Indicated)
Every FDA record for GGC TWN. Co., Ltd.
18 records, newest first. Each line links to the FDA page it came from.
2020
2019
- InspectionInspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
- Import refusalRefused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)HISTAMINEEntry 802-0072765-1Source
- Import refusalRefused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)FILTHYEntry 906-0219117-6Source
- Import alert listingListed on Import Alert 16-105red listTunaSource
2018
- Import refusalSource
Refused, 5 lines in one entry: Tuna (albacore, yellowfin, bluefin, skipjack, etc.)HISTAMINEFILTHYEntry AQZ-0447211-7Show 5 linesHide lines
- Refused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)HISTAMINEFILTHYEntry AQZ-0447211-7Source
- Refused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)HISTAMINEFILTHYEntry AQZ-0447211-7Source
- Refused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)HISTAMINEFILTHYEntry AQZ-0447211-7Source
- Refused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)HISTAMINEFILTHYEntry AQZ-0447211-7Source
- Refused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)HISTAMINEFILTHYEntry AQZ-0447211-7Source
- Import refusalSource
Refused, 3 lines in one entry: Tuna (albacore, yellowfin, bluefin, skipjack, etc.)FILTHYEntry BDD-0676664-2Show 3 linesHide lines
- Import refusalSource
Refused, 2 lines in one entry: Tuna (albacore, yellowfin, bluefin, skipjack, etc.)FILTHYEntry HK1-0235707-4Show 2 linesHide lines
- Import refusalRefused, Tuna (albacore, yellowfin, bluefin, skipjack, etc.)FILTHYEntry 334-3802036-5Source
2013
- InspectionInspection classified VAI (Voluntary Action Indicated)Foodborne Biological HazardsSource
2009
- 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.
- HISTAMINE7 refused lines
Histamine
The product appeared to contain histamine in a quantity that ordinarily makes it injurious to health.
Questions about GGC TWN. Co., Ltd.
- Is GGC TWN. Co., Ltd. on an FDA import alert?
- Yes. As of October 26, 2026, GGC TWN. Co., Ltd. is on the red list of FDA Import Alert 16-105, “Fish products: decomposition, histamine or indole”, for tuna; FDA published the listing on February 1, 2019.
- Has FDA refused shipments from GGC TWN. Co., Ltd.?
- Yes. FDA refused 14 shipment lines from GGC TWN. Co., Ltd. between February 8, 2018 and March 4, 2020. The most recent, on March 4, 2020, was tuna (albacore, yellowfin, bluefin, skipjack, etc.), charged as HISTAMINE (histamine).
- Why did FDA refuse GGC TWN. Co., Ltd.'s shipments?
- The most frequent charges are FILTHY (filthy, putrid or decomposed substance, 12 lines) and HISTAMINE (histamine, 7 lines).
- When was GGC TWN. Co., Ltd. last inspected by FDA?
- FDA's most recent inspection of GGC TWN. Co., Ltd. with a final classification is dated December 17, 2019 and was classified VAI (Voluntary Action Indicated).
- What is GGC TWN. Co., Ltd.'s FEI number?
- GGC TWN. Co., Ltd.'s FDA Establishment Identifier (FEI) is 3004264815.
- Can shipments from GGC TWN. Co., Ltd. still enter the U.S.?
- Shipments of tuna from GGC TWN. 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.