Przetworstwo Ryb Proryb
FDA import alert and refusal historyRumia, PolandFEI 3002855360
As of October 25, 2026, Przetworstwo Ryb Proryb (Rumia, Poland) is on the red list of FDA Import Alert 16-120 (Seafood from processors not in compliance with HACCP) for pickled herring, published by FDA on June 28, 2012, and has no FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 16-120 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- Classified OAI (Official Action Indicated)
Every FDA record for Przetworstwo Ryb Proryb
2 records, newest first. Each line links to the FDA page it came from.
2012
- Import alert listingListed on Import Alert 16-120red listPickled HerringSource
- InspectionInspection classified OAI (Official Action Indicated)Foodborne Biological HazardsSource
Questions about Przetworstwo Ryb Proryb
- Is Przetworstwo Ryb Proryb on an FDA import alert?
- Yes. As of October 25, 2026, Przetworstwo Ryb Proryb is on the red list of FDA Import Alert 16-120, “Seafood from processors not in compliance with HACCP”, for pickled herring; FDA published the listing on June 28, 2012.
- Has FDA refused shipments from Przetworstwo Ryb Proryb?
- No FDA import refusals for Przetworstwo Ryb Proryb appear in FDA's refusal data since October 2016, as of October 25, 2026.
- When was Przetworstwo Ryb Proryb last inspected by FDA?
- FDA's most recent inspection of Przetworstwo Ryb Proryb with a final classification is dated February 7, 2012 and was classified OAI (Official Action Indicated).
- What is Przetworstwo Ryb Proryb's FEI number?
- Przetworstwo Ryb Proryb's FDA Establishment Identifier (FEI) is 3002855360.
- Can shipments from Przetworstwo Ryb Proryb still enter the U.S.?
- Shipments of pickled herring from Przetworstwo Ryb Proryb can be detained without physical examination under Import Alert 16-120; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).
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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.