SupplierRadar

Guangzhou Yan Xiang Co, LTD

FDA import alert and refusal historyGuangzhou, ChinaFEI 3009824526

Watch this supplier

Watch this supplier

Get an email when FDA publishes anything new on Guangzhou Yan Xiang Co, LTD.

Enter your work email and confirm with the link we send. Your first supplier is free, with no password and no card.

Example subjectGuangzhou Yan Xiang Co, LT added to Import Alert 16-129 (red list)

Free for one supplier. No password, no card.

As of October 26, 2026, Guangzhou Yan Xiang Co, LTD (Guangzhou, China) is on the red list of FDA Import Alert 54-16 (Foods/supplements with active pharmaceutical ingredient) for ultimate formula bee pollen capsules, published by FDA on May 19, 2015, 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 Guangzhou Yan Xiang Co, LTD

1 record, newest first. Each line links to the FDA page it came from.

2015

  1. Import alert listing
    Listed on Import Alert 54-16red listUltimate Formula Bee Pollen Capsules
    Source

Questions about Guangzhou Yan Xiang Co, LTD

Is Guangzhou Yan Xiang Co, LTD on an FDA import alert?
Yes. As of October 26, 2026, Guangzhou Yan Xiang Co, LTD is on the red list of FDA Import Alert 54-16, “Foods/supplements with active pharmaceutical ingredient”, for ultimate formula bee pollen capsules; FDA published the listing on May 19, 2015.
Has FDA refused shipments from Guangzhou Yan Xiang Co, LTD?
No FDA import refusals for Guangzhou Yan Xiang Co, LTD appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is Guangzhou Yan Xiang Co, LTD's FEI number?
Guangzhou Yan Xiang Co, LTD's FDA Establishment Identifier (FEI) is 3009824526.
Can shipments from Guangzhou Yan Xiang Co, LTD still enter the U.S.?
Shipments of ultimate formula bee pollen capsules from Guangzhou Yan Xiang Co, LTD can be detained without physical examination under Import Alert 54-16; 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).

Buying from Guangzhou Yan Xiang Co, LTD?

Watch it and get the FDA record the day it changes. Free for one supplier.

Watch this supplier

Watch this supplier

Get an email when FDA publishes anything new on Guangzhou Yan Xiang Co, LTD.

Enter your work email and confirm with the link we send. Your first supplier is free, with no password and no card.

Example subjectGuangzhou Yan Xiang Co, LT added to Import Alert 16-129 (red list)

Free for one supplier. No password, no card.

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.