SupplierRadar

Rugen Fisch GMBH

FDA import alert and refusal historySassnitz, GermanyFEI 1000651397

Watch this supplier

Watch this supplier

Get an email when FDA publishes anything new on Rugen Fisch GMBH.

Enter your work email and confirm with the link we send. Your first supplier is free, with no password and no card.

Example subjectRugen Fisch GMB added to Import Alert 16-129 (red list)

Free for one supplier. No password, no card.

As of October 26, 2026, Rugen Fisch GMBH is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on December 10, 2019, 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
Cod · NO PROCESS
Last warning letter
None found
Last inspection
Classified VAI (Voluntary Action Indicated)

Every FDA record for Rugen Fisch GMBH

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

2019

  1. Import refusal
    Refused, CodNO PROCESSEntry 734-0087036-3
    Source

2013

  1. Inspection
    Inspection classified VAI (Voluntary Action Indicated)Foodborne Biological Hazards
    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 Rugen Fisch GMBH

Is Rugen Fisch GMBH on an FDA import alert?
No listing for Rugen Fisch GMBH appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Germany page.
Has FDA refused shipments from Rugen Fisch GMBH?
Yes. FDA refused 1 shipment line from Rugen Fisch GMBH on December 10, 2019. The most recent, on December 10, 2019, was cod, charged as NO PROCESS (no scheduled process filed).
Why did FDA refuse Rugen Fisch GMBH's shipments?
The most frequent charge is NO PROCESS (no scheduled process filed, 1 line).
When was Rugen Fisch GMBH last inspected by FDA?
FDA's most recent inspection of Rugen Fisch GMBH with a final classification is dated February 19, 2013 and was classified VAI (Voluntary Action Indicated).
What is Rugen Fisch GMBH's FEI number?
Rugen Fisch GMBH's FDA Establishment Identifier (FEI) is 1000651397.

Buying from Rugen Fisch GMBH?

Watch it and get the FDA record the day it changes. Free for one supplier.

Watch this supplier

Watch this supplier

Get an email when FDA publishes anything new on Rugen Fisch GMBH.

Enter your work email and confirm with the link we send. Your first supplier is free, with no password and no card.

Example subjectRugen Fisch GMB added to Import Alert 16-129 (red list)

Free for one supplier. No password, no card.

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.