Great Oasis Enterprises
FDA import alert and refusal historyMumbai, IndiaFEI 3004477548
As of October 26, 2026, Great Oasis Enterprises (Mumbai, India) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for crackers (non filled) n.e.c.; nut plain cookies,biscuits and wafers; plain cookies,biscuits and wafers, n.e.c., published by FDA on September 18, 2009, 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 Great Oasis Enterprises
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 45-02red listCrackers (Non Filled) N.E.C.; Nut Plain Cookies,Biscuits and Wafers; Plain Cookies,Biscuits and Wafers, N.E.C.Source
Questions about Great Oasis Enterprises
- Is Great Oasis Enterprises on an FDA import alert?
- Yes. As of October 26, 2026, Great Oasis Enterprises is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for crackers (non filled) n.e.c.; nut plain cookies,biscuits and wafers; plain cookies,biscuits and wafers, n.e.c.; FDA published the listing on September 18, 2009.
- Has FDA refused shipments from Great Oasis Enterprises?
- No FDA import refusals for Great Oasis Enterprises appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Great Oasis Enterprises's FEI number?
- Great Oasis Enterprises's FDA Establishment Identifier (FEI) is 3004477548.
- Can shipments from Great Oasis Enterprises still enter the U.S.?
- Shipments of crackers (non filled) n.e.c.; nut plain cookies,biscuits and wafers; plain cookies,biscuits and wafers, n.e.c. from Great Oasis Enterprises 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.