G-I-T
FDA import alert and refusal historyTbilisi, GeorgiaFEI 3030656349
As of October 26, 2026, G-I-T (Tbilisi, Georgia) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for mini fruit bar, published by FDA on June 26, 2024, and has 4 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
- Mixed fruit, dried or paste, n.e.c., · UNSAFE COL
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for G-I-T
5 records, newest first. Each line links to the FDA page it came from.
2026
- Import refusalSource
Refused, 2 lines in one entry: Mixed fruit, dried or paste, n.e.c.,UNSAFE COLCOLOR LBLGEntry ADR-0049107-8Show 2 linesHide lines
- Refused, Mixed fruit, dried or paste, n.e.c.,UNSAFE COLEntry ADR-0049107-8Source
- Refused, Mixed fruit, dried or paste, n.e.c.,COLOR LBLGEntry ADR-0049107-8Source
2024
- Import refusalSource
Refused, 2 lines in one entry: Mixed fruit, dried or paste, n.e.c.,UNSAFE COLLIST INGRELACKS FIRMLACKS N/CEntry ADR-0048095-6Show 2 linesHide lines
- Refused, Mixed fruit, dried or paste, n.e.c.,UNSAFE COLLIST INGRELACKS FIRMLACKS N/CUSUAL NAMELABELINGEntry ADR-0048095-6Source
- Refused, Mixed fruit, dried or paste, n.e.c.,UNSAFE COLLIST INGRELACKS FIRMLACKS N/CUSUAL NAMELABELINGEntry ADR-0048095-6Source
- Import alert listingListed on Import Alert 45-02red listMini Fruit BarSource
Refusal charges, in plain English
- UNSAFE COL3 refused lines
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.
- LABELING2 refused lines
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.
- LACKS FIRM2 refused lines
Manufacturer name and address missing
The packaged product's label appeared not to show the name and place of business of the manufacturer, packer, or distributor.
- LACKS N/C2 refused lines
Net quantity statement missing
The packaged food appeared not to carry an accurate statement of the quantity of contents, such as net weight, measure, or count, on its label.
- LIST INGRE2 refused lines
Ingredients not listed
The product is made from two or more ingredients and the label appeared not to list the common or usual name of each one (or, for a juice beverage, the percentage of juice).
- USUAL NAME2 refused lines
Common or usual name missing
The label appeared not to show the common or usual name of the food.
- COLOR LBLG1 refused line
Artificial coloring not declared
The product appeared to contain an artificial coloring without labeling that states that fact.
Questions about G-I-T
- Is G-I-T on an FDA import alert?
- Yes. As of October 26, 2026, G-I-T is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for mini fruit bar; FDA published the listing on June 26, 2024.
- Has FDA refused shipments from G-I-T?
- Yes. FDA refused 4 shipment lines from G-I-T between September 19, 2024 and June 4, 2026. The most recent, on June 4, 2026, was mixed fruit, dried or paste, n.e.c.,, charged as UNSAFE COL (color additive unsafe under section 721).
- Why did FDA refuse G-I-T's shipments?
- The most frequent charges are UNSAFE COL (color additive unsafe under section 721, 3 lines) and LABELING (fair packaging and labeling act, 2 lines).
- What is G-I-T's FEI number?
- G-I-T's FDA Establishment Identifier (FEI) is 3030656349.
- Can shipments from G-I-T still enter the U.S.?
- Shipments of mini fruit bar from G-I-T 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.