Amritsarian di Hatti
FDA import alert and refusal historyNew Delhi, IndiaFEI 3015353797
Recorded by FDA as AMRITSARIAN DI HATTI
As of October 26, 2026, Amritsarian di Hatti (New Delhi, India) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for sabudana (tapica sago) fryums snack, published by FDA on January 16, 2026, 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 45-02 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- Classified NAI (No Action Indicated)
Every FDA record for Amritsarian di Hatti
2 records, newest first. Each line links to the FDA page it came from.
2026
- Import alert listingListed on Import Alert 45-02red listSabudana (Tapica Sago) Fryums SnackSource
2025
- InspectionInspection classified NAI (No Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
Questions about Amritsarian di Hatti
- Is Amritsarian di Hatti on an FDA import alert?
- Yes. As of October 26, 2026, Amritsarian di Hatti is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for sabudana (tapica sago) fryums snack; FDA published the listing on January 16, 2026.
- Has FDA refused shipments from Amritsarian di Hatti?
- No FDA import refusals for Amritsarian di Hatti appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Amritsarian di Hatti last inspected by FDA?
- FDA's most recent inspection of Amritsarian di Hatti with a final classification is dated January 22, 2025 and was classified NAI (No Action Indicated).
- What is Amritsarian di Hatti's FEI number?
- Amritsarian di Hatti's FDA Establishment Identifier (FEI) is 3015353797.
- Can shipments from Amritsarian di Hatti still enter the U.S.?
- Shipments of sabudana (tapica sago) fryums snack from Amritsarian di Hatti can be detained without physical examination under Import Alert 45-02; 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.