SAS Enterprises
FDA import alert and refusal historyNew Delhi, IndiaFEI 3027562316
As of October 26, 2026, SAS Enterprises (New Delhi, India) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for mouth freshener rose saunf; new tree paan candy; khajoor mix soft candy, published by FDA on July 2, 2026, 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
- Classified NAI (No Action Indicated)
Every FDA record for SAS Enterprises
2 records, newest first. Each line links to the FDA page it came from.
2026
- Import alert listingListed on Import Alert 45-02red listMouth Freshener ROSE SAUNF; New Tree Paan Candy; Khajoor mix soft candySource
- InspectionInspection classified NAI (No Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
Questions about SAS Enterprises
- Is SAS Enterprises on an FDA import alert?
- Yes. As of October 26, 2026, SAS Enterprises is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for mouth freshener rose saunf; new tree paan candy; khajoor mix soft candy; FDA published the listing on July 2, 2026.
- Has FDA refused shipments from SAS Enterprises?
- No FDA import refusals for SAS Enterprises appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was SAS Enterprises last inspected by FDA?
- FDA's most recent inspection of SAS Enterprises with a final classification is dated April 24, 2026 and was classified NAI (No Action Indicated).
- What is SAS Enterprises's FEI number?
- SAS Enterprises's FDA Establishment Identifier (FEI) is 3027562316.
- Can shipments from SAS Enterprises still enter the U.S.?
- Shipments of mouth freshener rose saunf; new tree paan candy; khajoor mix soft candy from SAS Enterprises 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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