Guangzhou Garden City (Biological) Health Food Factory
FDA import alert and refusal historyGuangzhou, ChinaFEI 3010764129
As of October 27, 2026, Guangzhou Garden City (Biological) Health Food Factory (Guangzhou, China) is on the red list of FDA Import Alert 54-16 (Foods/supplements with active pharmaceutical ingredient) for la jiao shou shen, published by FDA on April 23, 2015, 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 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 Garden City (Biological) Health Food Factory
1 record, newest first. Each line links to the FDA page it came from.
2015
- Import alert listingListed on Import Alert 54-16red listLa Jiao Shou ShenSource
Questions about Guangzhou Garden City (Biological) Health Food Factory
- Is Guangzhou Garden City (Biological) Health Food Factory on an FDA import alert?
- Yes. As of October 27, 2026, Guangzhou Garden City (Biological) Health Food Factory is on the red list of FDA Import Alert 54-16, “Foods/supplements with active pharmaceutical ingredient”, for la jiao shou shen; FDA published the listing on April 23, 2015.
- Has FDA refused shipments from Guangzhou Garden City (Biological) Health Food Factory?
- No FDA import refusals for Guangzhou Garden City (Biological) Health Food Factory appear in FDA's refusal data since October 2016, as of October 27, 2026.
- What is Guangzhou Garden City (Biological) Health Food Factory's FEI number?
- Guangzhou Garden City (Biological) Health Food Factory's FDA Establishment Identifier (FEI) is 3010764129.
- Can shipments from Guangzhou Garden City (Biological) Health Food Factory still enter the U.S.?
- Shipments of la jiao shou shen from Guangzhou Garden City (Biological) Health Food Factory 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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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.