Hai Ning Qi Shen
FDA import alert and refusal historyZhejiang Province, ChinaFEI 3004490259
As of October 26, 2026, Hai Ning Qi Shen (Zhejiang Province, China) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for drink mix goji berry chrysanthemum honey crystal; drink mix jujube longan honey crystal, published by FDA on July 12, 2013, 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 99-08 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Hai Ning Qi Shen
1 record, newest first. Each line links to the FDA page it came from.
2013
- Import alert listingListed on Import Alert 99-08red listDrink Mix Goji Berry Chrysanthemum Honey Crystal; Drink Mix Jujube longan Honey CrystalSource
Questions about Hai Ning Qi Shen
- Is Hai Ning Qi Shen on an FDA import alert?
- Yes. As of October 26, 2026, Hai Ning Qi Shen is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for drink mix goji berry chrysanthemum honey crystal; drink mix jujube longan honey crystal; FDA published the listing on July 12, 2013.
- Has FDA refused shipments from Hai Ning Qi Shen?
- No FDA import refusals for Hai Ning Qi Shen appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Hai Ning Qi Shen's FEI number?
- Hai Ning Qi Shen's FDA Establishment Identifier (FEI) is 3004490259.
- Can shipments from Hai Ning Qi Shen still enter the U.S.?
- Shipments of drink mix goji berry chrysanthemum honey crystal; drink mix jujube longan honey crystal from Hai Ning Qi Shen can be detained without physical examination under Import Alert 99-08; 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.