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M.J.D. Seafood S.A.

FDA import alert and refusal historyGuayaquil, EcuadorFEI 3010778176

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Example subjectM.J.D. Seafood S.A added to Import Alert 16-129 (red list)

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As of October 26, 2026, M.J.D. Seafood S.A. is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines on January 7, 2021, most often for insanitary manufacturing, processing or packing (MFR INSAN).

Data from FDA public records, last checked . Request a correction

Current status

Import alerts
Not listed
Last import refusal
Clams · MFR INSAN
Last warning letter
None found
Last inspection
None on record

Every FDA record for M.J.D. Seafood S.A.

2 records, newest first. Each line links to the FDA page it came from.

2021

  1. Import refusal
    Refused, 2 lines in one entry: ClamsMFR INSANEntry 9AG-0045398-7Show 2 lines
    Source

Refusal charges, in plain English

  • MFR INSAN2 refused lines

    Insanitary manufacturing, processing or packing

    The product appeared to have been manufactured, processed, or packed under insanitary conditions, which is a ground for refusal under section 801(a)(1) of the FD&C Act.

Questions about M.J.D. Seafood S.A.

Is M.J.D. Seafood S.A. on an FDA import alert?
No listing for M.J.D. Seafood S.A. appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Ecuador page.
Has FDA refused shipments from M.J.D. Seafood S.A.?
Yes. FDA refused 2 shipment lines from M.J.D. Seafood S.A. on January 7, 2021. The most recent, on January 7, 2021, was clams, charged as MFR INSAN (insanitary manufacturing, processing or packing).
Why did FDA refuse M.J.D. Seafood S.A.'s shipments?
The most frequent charge is MFR INSAN (insanitary manufacturing, processing or packing, 2 lines).
What is M.J.D. Seafood S.A.'s FEI number?
M.J.D. Seafood S.A.'s FDA Establishment Identifier (FEI) is 3010778176.

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Example subjectM.J.D. Seafood S.A added to Import Alert 16-129 (red list)

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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.