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Pe

FDA import alert and refusal historySvitlovodsk, UkraineFEI 3016875604

Recorded by FDA as PE

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As of October 25, 2026, Pe is not on any FDA import alert in SupplierRadar's records; FDA refused 21 of its shipment lines on November 30, 2020, most often for processor not registered for canned or acidified foods (NEEDS FCE).

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

Current status

Import alerts
Not listed
Last import refusal
Catsup · NEEDS FCE
Last warning letter
None found
Last inspection
None on record

Every FDA record for Pe

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

2020

  1. Import refusal
    Refused, 21 lines in one entry: Catsup; Mustard, prepared and 3 moreNEEDS FCENO PROCESSEntry 9AJ-0819230-2Show 21 lines
    Source

Refusal charges, in plain English

  • NEEDS FCE21 refused lines

    Processor not registered for canned or acidified foods

    The manufacturer appeared not to be registered with FDA as a low-acid canned food or acidified food processor, as 21 CFR 108.25 and 108.35 require.

  • NO PROCESS21 refused lines

    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 Pe

Is Pe on an FDA import alert?
No listing for Pe appears in the FDA import alerts SupplierRadar checked on October 25, 2026. Country-wide alerts may still apply to its products; see the Ukraine page.
Has FDA refused shipments from Pe?
Yes. FDA refused 21 shipment lines from Pe on November 30, 2020. The most recent, on November 30, 2020, was catsup, charged as NEEDS FCE (processor not registered for canned or acidified foods).
Why did FDA refuse Pe's shipments?
The most frequent charges are NEEDS FCE (processor not registered for canned or acidified foods, 21 lines) and NO PROCESS (no scheduled process filed, 21 lines).
What is Pe's FEI number?
Pe's FDA Establishment Identifier (FEI) is 3016875604.

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Example subjectP 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.