Mat Ddeul An Co Ltd
FDA import alert and refusal historySaha, South KoreaFEI 3022147403
Recorded by FDA as MAT DDEUL AN CO LTD
As of October 25, 2026, Mat Ddeul An Co Ltd is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines on October 4, 2023, most often for imptrhaccp (IMPTRHACCP).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Surimi (used for further processing into imitation seafood) · IMPTRHACCP
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Mat Ddeul An Co Ltd
2 records, newest first. Each line links to the FDA page it came from.
2023
- Import refusalSource
Refused, 2 lines in one entry: Surimi (used for further processing into imitation seafood); Fish cakes, balls, etc., n.e.c.IMPTRHACCPEntry 677-0333830-0Show 2 linesHide lines
- Refused, Surimi (used for further processing into imitation seafood)IMPTRHACCPEntry 677-0333830-0Source
- Refused, Fish cakes, balls, etc., n.e.c.IMPTRHACCPEntry 677-0333830-0Source
Refusal charges, in plain English
- IMPTRHACCP2 refused lines
IMPTRHACCP
Questions about Mat Ddeul An Co Ltd
- Is Mat Ddeul An Co Ltd on an FDA import alert?
- No listing for Mat Ddeul An Co Ltd appears in the FDA import alerts SupplierRadar checked on October 25, 2026. Country-wide alerts may still apply to its products; see the South Korea page.
- Has FDA refused shipments from Mat Ddeul An Co Ltd?
- Yes. FDA refused 2 shipment lines from Mat Ddeul An Co Ltd on October 4, 2023. The most recent, on October 4, 2023, was surimi (used for further processing into imitation seafood), charged as IMPTRHACCP (imptrhaccp).
- Why did FDA refuse Mat Ddeul An Co Ltd's shipments?
- The most frequent charge is IMPTRHACCP (imptrhaccp, 2 lines).
- What is Mat Ddeul An Co Ltd's FEI number?
- Mat Ddeul An Co Ltd's FDA Establishment Identifier (FEI) is 3022147403.
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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.