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Shenzhen Baoyitong

FDA import alert and refusal historyShenzhen, ChinaFEI 3012778227

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Example subjectShenzhen Baoyiton added to Import Alert 16-129 (red list)

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As of October 25, 2026, Shenzhen Baoyitong (Shenzhen, China) is on the red list of FDA Import Alert 54-16 (Foods/supplements with active pharmaceutical ingredient) for aulijing zi su body fat health ii dietary supplement, published by FDA on October 26, 2016, 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 Shenzhen Baoyitong

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

2016

  1. Import alert listing
    Listed on Import Alert 54-16red listAulijing Zi Su Body Fat Health II Dietary Supplement
    Source

Questions about Shenzhen Baoyitong

Is Shenzhen Baoyitong on an FDA import alert?
Yes. As of October 25, 2026, Shenzhen Baoyitong is on the red list of FDA Import Alert 54-16, “Foods/supplements with active pharmaceutical ingredient”, for aulijing zi su body fat health ii dietary supplement; FDA published the listing on October 26, 2016.
Has FDA refused shipments from Shenzhen Baoyitong?
No FDA import refusals for Shenzhen Baoyitong appear in FDA's refusal data since October 2016, as of October 25, 2026.
What is Shenzhen Baoyitong's FEI number?
Shenzhen Baoyitong's FDA Establishment Identifier (FEI) is 3012778227.
Can shipments from Shenzhen Baoyitong still enter the U.S.?
Shipments of aulijing zi su body fat health ii dietary supplement from Shenzhen Baoyitong 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).

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Example subjectShenzhen Baoyiton 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.