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Sia Piejura

FDA import alert and refusal historyNicas Pagasts, LatviaFEI 3010896348

Recorded by FDA as SIA PIEJURA

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Example subjectSia Piejur added to Import Alert 16-129 (red list)

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As of October 26, 2026, Sia Piejura is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on June 20, 2018, most often for no scheduled process filed (NO PROCESS).

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

Current status

Import alerts
Not listed
Last import refusal
Sardines (brisling, sprats, pilchards, etc.), hot smoked, fish · NO PROCESS
Last warning letter
None found
Last inspection
None on record

Every FDA record for Sia Piejura

1 record, newest first. Each line links to the FDA page it came from.

2018

  1. Import refusal
    Refused, Sardines (brisling, sprats, pilchards, etc.), hot smoked, fishNO PROCESSEntry 9AJ-0811018-9
    Source

Refusal charges, in plain English

  • NO PROCESS1 refused line

    No scheduled process filed

    The manufacturer appeared not to have filed a scheduled process with FDA, which 21 CFR Part 108 requires for low-acid canned and acidified foods, so the product is treated as made under insanitary conditions.

Questions about Sia Piejura

Is Sia Piejura on an FDA import alert?
No listing for Sia Piejura appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Latvia page.
Has FDA refused shipments from Sia Piejura?
Yes. FDA refused 1 shipment line from Sia Piejura on June 20, 2018. The most recent, on June 20, 2018, was sardines (brisling, sprats, pilchards, etc.), hot smoked, fish, charged as NO PROCESS (no scheduled process filed).
Why did FDA refuse Sia Piejura's shipments?
The most frequent charge is NO PROCESS (no scheduled process filed, 1 line).
What is Sia Piejura's FEI number?
Sia Piejura's FDA Establishment Identifier (FEI) is 3010896348.

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Example subjectSia Piejur 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.