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Phuket Dongher Trading Co., Ltd.

FDA import alert and refusal historyMueang Phuket, ThailandFEI 3004138610

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Example subjectPhuket Dongher Trading Co., Ltd added to Import Alert 16-129 (red list)

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As of October 26, 2026, Phuket Dongher Trading Co., Ltd. has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on March 27, 2019, was classified NAI (No Action Indicated).

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

Current status

Import alerts
Not listed
Last import refusal
None since October 2016
Last warning letter
None found
Last inspection
Classified NAI (No Action Indicated)

Every FDA record for Phuket Dongher Trading Co., Ltd.

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

2019

  1. Inspection
    Inspection classified NAI (No Action Indicated)Foodborne Biological Hazards
    Source

2009

  1. Inspection
    Inspection classified VAI (Voluntary Action Indicated)Foodborne Biological Hazards
    Source

Questions about Phuket Dongher Trading Co., Ltd.

Is Phuket Dongher Trading Co., Ltd. on an FDA import alert?
No listing for Phuket Dongher Trading Co., Ltd. appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Thailand page.
Has FDA refused shipments from Phuket Dongher Trading Co., Ltd.?
No FDA import refusals for Phuket Dongher Trading Co., Ltd. appear in FDA's refusal data since October 2016, as of October 26, 2026.
When was Phuket Dongher Trading Co., Ltd. last inspected by FDA?
FDA's most recent inspection of Phuket Dongher Trading Co., Ltd. with a final classification is dated March 27, 2019 and was classified NAI (No Action Indicated).
What is Phuket Dongher Trading Co., Ltd.'s FEI number?
Phuket Dongher Trading Co., Ltd.'s FDA Establishment Identifier (FEI) is 3004138610.

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Example subjectPhuket Dongher Trading Co., Ltd 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.