Hershey India
FDA import alert and refusal historyMandideep, IndiaFEI 3006706593
As of October 26, 2026, Hershey India (Mandideep, India) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for custard powder vanilla; custard, french, not vanilla or vanillin flavored; custard powder vanilla (brown and polson); kissan mango jam, published by FDA on January 20, 2010, 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 Hershey India
1 record, newest first. Each line links to the FDA page it came from.
2010
- Import alert listingListed on Import Alert 45-02red listCustard Powder Vanilla; Custard, French, Not Vanilla or Vanillin Flavored; Custard Powder Vanilla (Brown and Polson); Kissan Mango JamSource
Questions about Hershey India
- Is Hershey India on an FDA import alert?
- Yes. As of October 26, 2026, Hershey India is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for custard powder vanilla; custard, french, not vanilla or vanillin flavored; custard powder vanilla (brown and polson); kissan mango jam; FDA published the listing on January 20, 2010.
- Has FDA refused shipments from Hershey India?
- No FDA import refusals for Hershey India appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Hershey India's FEI number?
- Hershey India's FDA Establishment Identifier (FEI) is 3006706593.
- Can shipments from Hershey India still enter the U.S.?
- Shipments of custard powder vanilla; custard, french, not vanilla or vanillin flavored; custard powder vanilla (brown and polson); kissan mango jam from Hershey 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.