Multi-I
FDA import alert and refusal historyAmsterdamamsterdam, NetherlandsFEI 3012183623
As of October 26, 2026, Multi-I (Amsterdamamsterdam, Netherlands) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for black amsterdam cannabis lollypops, published by FDA on June 21, 2017, 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
- Lollipop (without chocolate) · LABELING
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Multi-I
2 records, newest first. Each line links to the FDA page it came from.
2017
- Import alert listingListed on Import Alert 45-02red listBlack Amsterdam Cannabis LollypopsSource
2016
Refusal charges, in plain English
- LABELING1 refused line
Fair Packaging and Labeling Act
The package appeared not to meet the Fair Packaging and Labeling Act because of the placement, form, or contents of a required label statement.
Questions about Multi-I
- Is Multi-I on an FDA import alert?
- Yes. As of October 26, 2026, Multi-I is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for black amsterdam cannabis lollypops; FDA published the listing on June 21, 2017.
- Has FDA refused shipments from Multi-I?
- Yes. FDA refused 1 shipment line from Multi-I on October 5, 2016. The most recent, on October 5, 2016, was lollipop (without chocolate), charged as LABELING (fair packaging and labeling act).
- Why did FDA refuse Multi-I's shipments?
- The most frequent charge is LABELING (fair packaging and labeling act, 1 line).
- What is Multi-I's FEI number?
- Multi-I's FDA Establishment Identifier (FEI) is 3012183623.
- Can shipments from Multi-I still enter the U.S.?
- Shipments of black amsterdam cannabis lollypops from Multi-I 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.