guangzhou p'product
FDA import alert and refusal historyGuangzhou, ChinaFEI 3004319550
As of October 25, 2026, guangzhou p'product (Guangzhou, China) is on the red list of FDA Import Alert 99-39 (Imported foods that appear to be misbranded) for herba plantaginis (plantain herb), published by FDA on April 5, 2023, is also listed on Import Alert 54-16 (red list), 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 99-39 · red listIA 54-16 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for guangzhou p'product
2 records, newest first. Each line links to the FDA page it came from.
2023
- Import alert listingListed on Import Alert 99-39red listHerba Plantaginis (Plantain Herb)Source
- Import alert listingListed on Import Alert 54-16red listHerba Plantaginis (Plantain Herb)Source
Questions about guangzhou p'product
- Is guangzhou p'product on an FDA import alert?
- Yes. As of October 25, 2026, guangzhou p'product is on the red list of FDA Import Alert 99-39, “Imported foods that appear to be misbranded”, for herba plantaginis (plantain herb); FDA published the listing on April 5, 2023.
- Has FDA refused shipments from guangzhou p'product?
- No FDA import refusals for guangzhou p'product appear in FDA's refusal data since October 2016, as of October 25, 2026.
- What is guangzhou p'product's FEI number?
- guangzhou p'product's FDA Establishment Identifier (FEI) is 3004319550.
- Can shipments from guangzhou p'product still enter the U.S.?
- Shipments of herba plantaginis (plantain herb) from guangzhou p'product can be detained without physical examination under Import Alert 99-39; 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.