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Nam Fong Factory

FDA import alert and refusal historyGaoming City Guangdong, ChinaFEI 1000336156

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Example subjectNam Fong Factor added to Import Alert 16-129 (red list)

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As of October 26, 2026, Nam Fong Factory (Gaoming City Guangdong, China) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for chinese ginseng, published by FDA on September 16, 2009, is also listed on Import Alert 99-19 (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 Nam Fong Factory

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

2009

  1. Import alert listing
    Listed on Import Alert 99-08red listChinese Ginseng
    Source
  2. Import alert listing
    Listed on Import Alert 99-19red listwhite pepper powder
    Source

Questions about Nam Fong Factory

Is Nam Fong Factory on an FDA import alert?
Yes. As of October 26, 2026, Nam Fong Factory is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for chinese ginseng; FDA published the listing on September 16, 2009.
Has FDA refused shipments from Nam Fong Factory?
No FDA import refusals for Nam Fong Factory appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is Nam Fong Factory's FEI number?
Nam Fong Factory's FDA Establishment Identifier (FEI) is 1000336156.
Can shipments from Nam Fong Factory still enter the U.S.?
Shipments of chinese ginseng from Nam Fong Factory can be detained without physical examination under Import Alert 99-08; 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 subjectNam Fong Factor 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.