Chielin Co Ltd
FDA import alert and refusal historyYao, JapanFEI 3003679331
As of October 26, 2026, Chielin Co Ltd (Yao, Japan) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for chewing gum, published by FDA on March 18, 2020, and has 1 FDA import refusal 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
- Chewing gum (without chocolate) · UNSAFE COL
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Chielin Co Ltd
2 records, newest first. Each line links to the FDA page it came from.
2025
- Import refusalRefused, Chewing gum (without chocolate)UNSAFE COLEntry 9ES-0095820-5Source
2020
- Import alert listingListed on Import Alert 45-02red listChewing gumSource
Refusal charges, in plain English
- UNSAFE COL1 refused line
Color additive unsafe under section 721
The product appeared to be, or to contain, a color additive that is unsafe within the meaning of section 721(a) of the FD&C Act, the section that governs which color additives may be used and how.
Questions about Chielin Co Ltd
- Is Chielin Co Ltd on an FDA import alert?
- Yes. As of October 26, 2026, Chielin Co Ltd is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for chewing gum; FDA published the listing on March 18, 2020.
- Has FDA refused shipments from Chielin Co Ltd?
- Yes. FDA refused 1 shipment line from Chielin Co Ltd on October 10, 2025. The most recent, on October 10, 2025, was chewing gum (without chocolate), charged as UNSAFE COL (color additive unsafe under section 721).
- Why did FDA refuse Chielin Co Ltd's shipments?
- The most frequent charge is UNSAFE COL (color additive unsafe under section 721, 1 line).
- What is Chielin Co Ltd's FEI number?
- Chielin Co Ltd's FDA Establishment Identifier (FEI) is 3003679331.
- Can shipments from Chielin Co Ltd still enter the U.S.?
- Shipments of chewing gum from Chielin Co Ltd 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.