China Heilongjiang Native Produce & Animal Products Imp&Exp
FDA import alert and refusal historyDalian, ChinaFEI 1000128394
As of October 26, 2026, China Heilongjiang Native Produce & Animal Products Imp&Exp (Dalian, China) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for honey, published by FDA on October 4, 2018, 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 China Heilongjiang Native Produce & Animal Products Imp&Exp
1 record, newest first. Each line links to the FDA page it came from.
2018
- Import alert listingListed on Import Alert 99-08red listHoneySource
Questions about China Heilongjiang Native Produce & Animal Products Imp&Exp
- Is China Heilongjiang Native Produce & Animal Products Imp&Exp on an FDA import alert?
- Yes. As of October 26, 2026, China Heilongjiang Native Produce & Animal Products Imp&Exp is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for honey; FDA published the listing on October 4, 2018.
- Has FDA refused shipments from China Heilongjiang Native Produce & Animal Products Imp&Exp?
- No FDA import refusals for China Heilongjiang Native Produce & Animal Products Imp&Exp appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is China Heilongjiang Native Produce & Animal Products Imp&Exp's FEI number?
- China Heilongjiang Native Produce & Animal Products Imp&Exp's FDA Establishment Identifier (FEI) is 1000128394.
- Can shipments from China Heilongjiang Native Produce & Animal Products Imp&Exp still enter the U.S.?
- Shipments of honey from China Heilongjiang Native Produce & Animal Products Imp&Exp 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.