Bombay Export
FDA import alert and refusal historyMumbai, IndiaFEI 3000281905
As of October 25, 2026, Bombay Export (Mumbai, India) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for soft drink, citrus fruit flavored, carbonated; soft drink, imitation fruit flavored, carbonated; fanta, 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 Bombay Export
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 45-02red listSoft Drink, Citrus Fruit Flavored, Carbonated; Soft Drink, Imitation Fruit Flavored, Carbonated; FantaSource
Questions about Bombay Export
- Is Bombay Export on an FDA import alert?
- Yes. As of October 25, 2026, Bombay Export is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for soft drink, citrus fruit flavored, carbonated; soft drink, imitation fruit flavored, carbonated; fanta; FDA published the listing on September 18, 2009.
- Has FDA refused shipments from Bombay Export?
- No FDA import refusals for Bombay Export appear in FDA's refusal data since October 2016, as of October 25, 2026.
- What is Bombay Export's FEI number?
- Bombay Export's FDA Establishment Identifier (FEI) is 3000281905.
- Can shipments from Bombay Export still enter the U.S.?
- Shipments of soft drink, citrus fruit flavored, carbonated; soft drink, imitation fruit flavored, carbonated; fanta from Bombay Export 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.