Limited Liability Company "Name Amangeldy"
FDA import alert and refusal historyAtyrau, KazakhstanFEI 3011816866
As of October 26, 2026, Limited Liability Company "Name Amangeldy" (Atyrau, Kazakhstan) is on the red list of FDA Import Alert 16-120 (Seafood from processors not in compliance with HACCP) for salted; dried fish, published by FDA on November 15, 2016, is also listed on Import Alert 16-74 (red list), 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 listIA 16-74 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Limited Liability Company "Name Amangeldy"
2 records, newest first. Each line links to the FDA page it came from.
2016
- Import alert listingListed on Import Alert 16-120red listSalted; Dried FishSource
- Import alert listingListed on Import Alert 16-74red listDried; salted bream; Roach Dry Eviscerated Salted Fish (Caspian Roach)Source
Questions about Limited Liability Company "Name Amangeldy"
- Is Limited Liability Company "Name Amangeldy" on an FDA import alert?
- Yes. As of October 26, 2026, Limited Liability Company "Name Amangeldy" is on the red list of FDA Import Alert 16-120, “Seafood from processors not in compliance with HACCP”, for salted; dried fish; FDA published the listing on November 15, 2016.
- Has FDA refused shipments from Limited Liability Company "Name Amangeldy"?
- No FDA import refusals for Limited Liability Company "Name Amangeldy" appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Limited Liability Company "Name Amangeldy"'s FEI number?
- Limited Liability Company "Name Amangeldy"'s FDA Establishment Identifier (FEI) is 3011816866.
- Can shipments from Limited Liability Company "Name Amangeldy" still enter the U.S.?
- Shipments of salted; dried fish from Limited Liability Company "Name Amangeldy" 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.