Samrat Namkeen PVT LTD
FDA import alert and refusal historyAhmedabad, IndiaFEI 3004318874
As of October 26, 2026, Samrat Namkeen PVT LTD is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on January 26, 2026, 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
- Tamarind, dried or paste · FILTHY
- Last warning letter
- None found
- Last inspection
- Classified VAI (Voluntary Action Indicated)
Every FDA record for Samrat Namkeen PVT LTD
2 records, newest first. Each line links to the FDA page it came from.
Refusal charges, in plain English
- FILTHY1 refused line
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 Samrat Namkeen PVT LTD
- Is Samrat Namkeen PVT LTD on an FDA import alert?
- No listing for Samrat Namkeen PVT LTD appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the India page.
- Has FDA refused shipments from Samrat Namkeen PVT LTD?
- Yes. FDA refused 1 shipment line from Samrat Namkeen PVT LTD on January 26, 2026. The most recent, on January 26, 2026, was tamarind, dried or paste, charged as FILTHY (filthy, putrid or decomposed substance).
- Why did FDA refuse Samrat Namkeen PVT LTD's shipments?
- The most frequent charge is FILTHY (filthy, putrid or decomposed substance, 1 line).
- When was Samrat Namkeen PVT LTD last inspected by FDA?
- FDA's most recent inspection of Samrat Namkeen PVT LTD with a final classification is dated November 15, 2018 and was classified VAI (Voluntary Action Indicated).
- What is Samrat Namkeen PVT LTD's FEI number?
- Samrat Namkeen PVT LTD's FDA Establishment Identifier (FEI) is 3004318874.
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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.