Hai Phong Honeybee
FDA import alert and refusal historyHo Chi Minh, VietnamFEI 3010470621
As of October 26, 2026, Hai Phong Honeybee (Ho Chi Minh, Vietnam) is on the red list of FDA Import Alert 99-47 (Foods that appear adulterated for economic gain) for honey, published by FDA on May 2, 2023, and has 1 FDA import refusal recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 99-47 · red list
- Last import refusal
- Honey · SUBSTITUTE
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Hai Phong Honeybee
2 records, newest first. Each line links to the FDA page it came from.
2023
- Import alert listingListed on Import Alert 99-47red listHoneySource
2022
- Import refusalRefused, HoneySUBSTITUTEEntry K30-2016152-9Source
Refusal charges, in plain English
- SUBSTITUTE1 refused line
SUBSTITUTE
Questions about Hai Phong Honeybee
- Is Hai Phong Honeybee on an FDA import alert?
- Yes. As of October 26, 2026, Hai Phong Honeybee is on the red list of FDA Import Alert 99-47, “Foods that appear adulterated for economic gain”, for honey; FDA published the listing on May 2, 2023.
- Has FDA refused shipments from Hai Phong Honeybee?
- Yes. FDA refused 1 shipment line from Hai Phong Honeybee on June 6, 2022. The most recent, on June 6, 2022, was honey, charged as SUBSTITUTE (substitute).
- Why did FDA refuse Hai Phong Honeybee's shipments?
- The most frequent charge is SUBSTITUTE (substitute, 1 line).
- What is Hai Phong Honeybee's FEI number?
- Hai Phong Honeybee's FDA Establishment Identifier (FEI) is 3010470621.
- Can shipments from Hai Phong Honeybee still enter the U.S.?
- Shipments of honey from Hai Phong Honeybee can be detained without physical examination under Import Alert 99-47; 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.