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Grybai Lt

FDA import alert and refusal historySirvintos, LithuaniaFEI 3013855739

Recorded by FDA as GRYBAI LT

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Example subjectGrybai L added to Import Alert 16-129 (red list)

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As of October 26, 2026, Grybai Lt is not on any FDA import alert in SupplierRadar's records; FDA refused 15 of its shipment lines on October 17, 2017, 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
Kidney bean · NO PROCESS
Last warning letter
None found
Last inspection
Classified NAI (No Action Indicated)

Every FDA record for Grybai Lt

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

2024

  1. Inspection
    Inspection classified NAI (No Action Indicated)Foodborne Biological Hazards
    Source

2017

  1. Import refusal
    Refused, 15 lines in one entry: Kidney bean; Root & tuber vegetable, n.e.c. and 11 moreNO PROCESSEntry 9UV-0754872-8Show 15 lines
    Source

Refusal charges, in plain English

  • NO PROCESS15 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 Grybai Lt

Is Grybai Lt on an FDA import alert?
No listing for Grybai Lt appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Lithuania page.
Has FDA refused shipments from Grybai Lt?
Yes. FDA refused 15 shipment lines from Grybai Lt on October 17, 2017. The most recent, on October 17, 2017, was kidney bean, charged as NO PROCESS (no scheduled process filed).
Why did FDA refuse Grybai Lt's shipments?
The most frequent charge is NO PROCESS (no scheduled process filed, 15 lines).
When was Grybai Lt last inspected by FDA?
FDA's most recent inspection of Grybai Lt with a final classification is dated September 18, 2024 and was classified NAI (No Action Indicated).
What is Grybai Lt's FEI number?
Grybai Lt's FDA Establishment Identifier (FEI) is 3013855739.

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Example subjectGrybai L 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.