Gwalia Sweets Private Limited
FDA import alert and refusal historyAhmedabad, IndiaFEI 3010075513
As of October 26, 2026, Gwalia Sweets Private Limited (Ahmedabad, India) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for anjeer cake; mango bites; rose bites; orange bites; pista madhuram; moong dal barfi; green mango delight; orange katari, published by FDA on September 30, 2024, 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
- None on record
Every FDA record for Gwalia Sweets Private Limited
1 record, newest first. Each line links to the FDA page it came from.
2024
- Import alert listingListed on Import Alert 45-02red listAnjeer cake; Mango Bites; Rose Bites; Orange Bites; PISTA MADHURAM; MOONG DAL BARFI; GREEN MANGO DELIGHT; Orange KatariSource
Questions about Gwalia Sweets Private Limited
- Is Gwalia Sweets Private Limited on an FDA import alert?
- Yes. As of October 26, 2026, Gwalia Sweets Private Limited is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for anjeer cake; mango bites; rose bites; orange bites; pista madhuram; moong dal barfi; green mango delight; orange katari; FDA published the listing on September 30, 2024.
- Has FDA refused shipments from Gwalia Sweets Private Limited?
- No FDA import refusals for Gwalia Sweets Private Limited appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Gwalia Sweets Private Limited's FEI number?
- Gwalia Sweets Private Limited's FDA Establishment Identifier (FEI) is 3010075513.
- Can shipments from Gwalia Sweets Private Limited still enter the U.S.?
- Shipments of anjeer cake; mango bites; rose bites; orange bites; pista madhuram; moong dal barfi; green mango delight; orange katari from Gwalia Sweets Private Limited 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.