Arctic Overseas
FDA import alert and refusal historyNew Delhi, IndiaFEI 3024732431
Recorded by FDA as ARCTIC OVERSEAS
As of October 26, 2026, Arctic Overseas (New Delhi, India) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for royal fusion; fruit mix shot; aam pappad pops; masala chuksi pops; satrangi fennel; paan candy shots; color pops; orangish pops; tangy pops; tooty fruity, published by FDA on October 27, 2023, 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 Arctic Overseas
1 record, newest first. Each line links to the FDA page it came from.
2023
- Import alert listingListed on Import Alert 45-02red listRoyal Fusion; Fruit Mix Shot; AAM PAPPAD POPS; Masala Chuksi Pops; Satrangi Fennel; Paan Candy Shots; Color Pops; Orangish Pops; Tangy Pops; Tooty FruitySource
Questions about Arctic Overseas
- Is Arctic Overseas on an FDA import alert?
- Yes. As of October 26, 2026, Arctic Overseas is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for royal fusion; fruit mix shot; aam pappad pops; masala chuksi pops; satrangi fennel; paan candy shots; color pops; orangish pops; tangy pops; tooty fruity; FDA published the listing on October 27, 2023.
- Has FDA refused shipments from Arctic Overseas?
- No FDA import refusals for Arctic Overseas appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Arctic Overseas's FEI number?
- Arctic Overseas's FDA Establishment Identifier (FEI) is 3024732431.
- Can shipments from Arctic Overseas still enter the U.S.?
- Shipments of royal fusion; fruit mix shot; aam pappad pops; masala chuksi pops; satrangi fennel; paan candy shots; color pops; orangish pops; tangy pops; tooty fruity from Arctic Overseas 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.