Sudip And Company
FDA import alert and refusal historyMumbai, IndiaFEI 3001690094
As of October 26, 2026, Sudip And Company (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; carbonated soft drink, 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 Sudip And Company
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; Carbonated Soft Drink, N.E.C.Source
Questions about Sudip And Company
- Is Sudip And Company on an FDA import alert?
- Yes. As of October 26, 2026, Sudip And Company 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; carbonated soft drink, n.e.c.; FDA published the listing on September 18, 2009.
- Has FDA refused shipments from Sudip And Company?
- No FDA import refusals for Sudip And Company appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Sudip And Company's FEI number?
- Sudip And Company's FDA Establishment Identifier (FEI) is 3001690094.
- Can shipments from Sudip And Company still enter the U.S.?
- Shipments of soft drink, citrus fruit flavored, carbonated; soft drink, imitation fruit flavored, carbonated; carbonated soft drink, n.e.c. from Sudip And Company 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.