Guang Zhou Native Produce I/E Co
FDA import alert and refusal historyGuangzhou, ChinaFEI 3001164050
As of October 26, 2026, Guang Zhou Native Produce I/E Co (Guangzhou, China) is on the red list of FDA Import Alert 99-21 (Foods with undeclared added sulfiting agents) for winter melon, dried or paste; winter melon, jam, jelly, preserves, marmalade, butter or candied, published by FDA on September 16, 2009, and has no FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 99-21 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Guang Zhou Native Produce I/E Co
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 99-21red listWinter Melon, Dried or Paste; Winter Melon, Jam, Jelly, Preserves, Marmalade, Butter or CandiedSource
Questions about Guang Zhou Native Produce I/E Co
- Is Guang Zhou Native Produce I/E Co on an FDA import alert?
- Yes. As of October 26, 2026, Guang Zhou Native Produce I/E Co is on the red list of FDA Import Alert 99-21, “Foods with undeclared added sulfiting agents”, for winter melon, dried or paste; winter melon, jam, jelly, preserves, marmalade, butter or candied; FDA published the listing on September 16, 2009.
- Has FDA refused shipments from Guang Zhou Native Produce I/E Co?
- No FDA import refusals for Guang Zhou Native Produce I/E Co appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Guang Zhou Native Produce I/E Co's FEI number?
- Guang Zhou Native Produce I/E Co's FDA Establishment Identifier (FEI) is 3001164050.
- Can shipments from Guang Zhou Native Produce I/E Co still enter the U.S.?
- Shipments of winter melon, dried or paste; winter melon, jam, jelly, preserves, marmalade, butter or candied from Guang Zhou Native Produce I/E Co can be detained without physical examination under Import Alert 99-21; 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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