Ra India
FDA import alert and refusal historyMaharashtra, IndiaFEI 3003360337
As of October 25, 2026, Ra India (Maharashtra, India) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for kissan mixed fruit jam; kissan mixed fruit jam 1/25/08; mint chutney; coriander chutney; green bhel chutney, 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 Ra India
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 45-02red listKissan Mixed fruit jam; Kissan Mixed Fruit Jam 1/25/08; mint chutney; coriander chutney; green bhel chutneySource
Questions about Ra India
- Is Ra India on an FDA import alert?
- Yes. As of October 25, 2026, Ra India is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for kissan mixed fruit jam; kissan mixed fruit jam 1/25/08; mint chutney; coriander chutney; green bhel chutney; FDA published the listing on September 18, 2009.
- Has FDA refused shipments from Ra India?
- No FDA import refusals for Ra India appear in FDA's refusal data since October 2016, as of October 25, 2026.
- What is Ra India's FEI number?
- Ra India's FDA Establishment Identifier (FEI) is 3003360337.
- Can shipments from Ra India still enter the U.S.?
- Shipments of kissan mixed fruit jam; kissan mixed fruit jam 1/25/08; mint chutney; coriander chutney; green bhel chutney from Ra India 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.