Le Thi Nguyet Anh
FDA import alert and refusal historyHo Chi Minh, VietnamFEI 3011589973
As of October 26, 2026, Le Thi Nguyet Anh (Ho Chi Minh, Vietnam) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for high quality preserved fruits, published by FDA on August 17, 2015, is also listed on Import Alert 99-21 (red list), 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 listIA 99-21 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Le Thi Nguyet Anh
2 records, newest first. Each line links to the FDA page it came from.
2015
- Import alert listingListed on Import Alert 99-08red listHigh quality preserved fruitsSource
- Import alert listingListed on Import Alert 99-21red listHigh Quality Preserved Fruits (Red Longan)/(Green LonganSource
Questions about Le Thi Nguyet Anh
- Is Le Thi Nguyet Anh on an FDA import alert?
- Yes. As of October 26, 2026, Le Thi Nguyet Anh is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for high quality preserved fruits; FDA published the listing on August 17, 2015.
- Has FDA refused shipments from Le Thi Nguyet Anh?
- No FDA import refusals for Le Thi Nguyet Anh appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Le Thi Nguyet Anh's FEI number?
- Le Thi Nguyet Anh's FDA Establishment Identifier (FEI) is 3011589973.
- Can shipments from Le Thi Nguyet Anh still enter the U.S.?
- Shipments of high quality preserved fruits from Le Thi Nguyet Anh 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.