IP Saltaganov A.V.
FDA import alert and refusal historyKalach-na-Donu, RussiaFEI 3011449401
As of October 26, 2026, IP Saltaganov A.V. (Kalach-na-Donu, Russia) is on the red list of FDA Import Alert 16-39 (Ready-to-eat seafood: Listeria monocytogenes) for eviscerated; dried herring, published by FDA on December 21, 2016, and has 1 FDA import refusal recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 16-39 · red list
- Last import refusal
- Herring · LISTERIA
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for IP Saltaganov A.V.
2 records, newest first. Each line links to the FDA page it came from.
2016
- Import refusalRefused, HerringLISTERIAEntry BQL-0048236-2Source
- Import alert listingListed on Import Alert 16-39red listEviscerated; Dried HerringSource
Refusal charges, in plain English
- LISTERIA1 refused line
Listeria monocytogenes
The product appeared to contain Listeria monocytogenes, which the law treats as a poisonous and deleterious substance that may make food injurious to health.
Questions about IP Saltaganov A.V.
- Is IP Saltaganov A.V. on an FDA import alert?
- Yes. As of October 26, 2026, IP Saltaganov A.V. is on the red list of FDA Import Alert 16-39, “Ready-to-eat seafood: Listeria monocytogenes”, for eviscerated; dried herring; FDA published the listing on December 21, 2016.
- Has FDA refused shipments from IP Saltaganov A.V.?
- Yes. FDA refused 1 shipment line from IP Saltaganov A.V. on December 27, 2016. The most recent, on December 27, 2016, was herring, charged as LISTERIA (listeria monocytogenes).
- Why did FDA refuse IP Saltaganov A.V.'s shipments?
- The most frequent charge is LISTERIA (listeria monocytogenes, 1 line).
- What is IP Saltaganov A.V.'s FEI number?
- IP Saltaganov A.V.'s FDA Establishment Identifier (FEI) is 3011449401.
- Can shipments from IP Saltaganov A.V. still enter the U.S.?
- Shipments of eviscerated; dried herring from IP Saltaganov A.V. can be detained without physical examination under Import Alert 16-39; 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.