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Goal Path Co.

FDA import alert and refusal historyGuangzhou,, ChinaFEI 3004161210

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Example subjectGoal Path Co added to Import Alert 16-129 (red list)

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As of October 25, 2026, Goal Path Co. (Guangzhou,, China) is on the red list of FDA Import Alert 99-45 (Foods that are or contain an unsafe food additive) for sweet potato; dried, published by FDA on May 12, 2025, is also listed on Import Alert 99-39 (red list), and has no FDA import refusals recorded since October 2016.

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

Current status

Last import refusal
None since October 2016
Last warning letter
None found
Last inspection
None on record

Every FDA record for Goal Path Co.

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

2025

  1. Import alert listing
    Listed on Import Alert 99-45red listSweet potato; dried
    Source
  2. Import alert listing
    Listed on Import Alert 99-39red listSweet Potato (Root & Tuber Vegetable), Ntrl/Artfcl Dried; Sweet Potato, Dried or Paste
    Source

Questions about Goal Path Co.

Is Goal Path Co. on an FDA import alert?
Yes. As of October 25, 2026, Goal Path Co. is on the red list of FDA Import Alert 99-45, “Foods that are or contain an unsafe food additive”, for sweet potato; dried; FDA published the listing on May 12, 2025.
Has FDA refused shipments from Goal Path Co.?
No FDA import refusals for Goal Path Co. appear in FDA's refusal data since October 2016, as of October 25, 2026.
What is Goal Path Co.'s FEI number?
Goal Path Co.'s FDA Establishment Identifier (FEI) is 3004161210.
Can shipments from Goal Path Co. still enter the U.S.?
Shipments of sweet potato; dried from Goal Path Co. can be detained without physical examination under Import Alert 99-45; 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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Example subjectGoal Path Co 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.