Red Chamber Argentina S.A.
FDA import alert and refusal historyPuerto Madryn, ArgentinaFEI 3011611990
As of October 26, 2026, Red Chamber Argentina S.A. is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines on January 24, 2023, most often for filthy, putrid or decomposed substance (FILTHY).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Hake · FILTHY
- Last warning letter
- None found
- Last inspection
- Classified NAI (No Action Indicated)
Every FDA record for Red Chamber Argentina S.A.
3 records, newest first. Each line links to the FDA page it came from.
Refusal charges, in plain English
- FILTHY2 refused lines
Filthy, putrid or decomposed substance
The product appeared to consist in whole or in part of a filthy, putrid, or decomposed substance, or to be otherwise unfit for food.
Questions about Red Chamber Argentina S.A.
- Is Red Chamber Argentina S.A. on an FDA import alert?
- No listing for Red Chamber Argentina S.A. appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Argentina page.
- Has FDA refused shipments from Red Chamber Argentina S.A.?
- Yes. FDA refused 2 shipment lines from Red Chamber Argentina S.A. on January 24, 2023. The most recent, on January 24, 2023, was hake, charged as FILTHY (filthy, putrid or decomposed substance).
- Why did FDA refuse Red Chamber Argentina S.A.'s shipments?
- The most frequent charge is FILTHY (filthy, putrid or decomposed substance, 2 lines).
- When was Red Chamber Argentina S.A. last inspected by FDA?
- FDA's most recent inspection of Red Chamber Argentina S.A. with a final classification is dated February 27, 2024 and was classified NAI (No Action Indicated).
- What is Red Chamber Argentina S.A.'s FEI number?
- Red Chamber Argentina S.A.'s FDA Establishment Identifier (FEI) is 3011611990.
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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.