United Dairy and Food Industries Company (UDFI)
FDA import alert and refusal historyAl Hudaydah, YemenFEI 3037696018
As of October 26, 2026, United Dairy and Food Industries Company (UDFI) (Al Hudaydah, Yemen) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for nana apple drink; nana mango drink; nana fruit drink, published by FDA on April 21, 2025, 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 45-02 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for United Dairy and Food Industries Company (UDFI)
1 record, newest first. Each line links to the FDA page it came from.
2025
- Import alert listingListed on Import Alert 45-02red listNANA Apple Drink; NANA Mango Drink; NANA Fruit DrinkSource
Questions about United Dairy and Food Industries Company (UDFI)
- Is United Dairy and Food Industries Company (UDFI) on an FDA import alert?
- Yes. As of October 26, 2026, United Dairy and Food Industries Company (UDFI) is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for nana apple drink; nana mango drink; nana fruit drink; FDA published the listing on April 21, 2025.
- Has FDA refused shipments from United Dairy and Food Industries Company (UDFI)?
- No FDA import refusals for United Dairy and Food Industries Company (UDFI) appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is United Dairy and Food Industries Company (UDFI)'s FEI number?
- United Dairy and Food Industries Company (UDFI)'s FDA Establishment Identifier (FEI) is 3037696018.
- Can shipments from United Dairy and Food Industries Company (UDFI) still enter the U.S.?
- Shipments of nana apple drink; nana mango drink; nana fruit drink from United Dairy and Food Industries Company (UDFI) can be detained without physical examination under Import Alert 45-02; 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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