Dps Co Ltd
FDA import alert and refusal historyYangon, MyanmarFEI 3013845379
Recorded by FDA as DPS CO LTD
As of October 26, 2026, Dps Co Ltd (Yangon, Myanmar) is on the red list of FDA Import Alert 99-19 (Food products: Salmonella) for betel leaf roll, published by FDA on July 3, 2018, 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 99-19 · red list
- Last import refusal
- Betel nut, shelled · SALMONELLA
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Dps Co Ltd
2 records, newest first. Each line links to the FDA page it came from.
2018
- Import refusalRefused, Betel nut, shelledSALMONELLAEntry HK1-0236564-8Source
- Import alert listingListed on Import Alert 99-19red listBetel Leaf rollSource
Refusal charges, in plain English
- SALMONELLA1 refused line
Salmonella
The product appeared to contain Salmonella, which the law treats as a poisonous and deleterious substance that may make food injurious to health.
Questions about Dps Co Ltd
- Is Dps Co Ltd on an FDA import alert?
- Yes. As of October 26, 2026, Dps Co Ltd is on the red list of FDA Import Alert 99-19, “Food products: Salmonella”, for betel leaf roll; FDA published the listing on July 3, 2018.
- Has FDA refused shipments from Dps Co Ltd?
- Yes. FDA refused 1 shipment line from Dps Co Ltd on August 21, 2018. The most recent, on August 21, 2018, was betel nut, shelled, charged as SALMONELLA (salmonella).
- Why did FDA refuse Dps Co Ltd's shipments?
- The most frequent charge is SALMONELLA (salmonella, 1 line).
- What is Dps Co Ltd's FEI number?
- Dps Co Ltd's FDA Establishment Identifier (FEI) is 3013845379.
- Can shipments from Dps Co Ltd still enter the U.S.?
- Shipments of betel leaf roll from Dps Co Ltd can be detained without physical examination under Import Alert 99-19; 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.