Baruqi Ltd
FDA import alert and refusal historyVazisubani, GeorgiaFEI 3013960831
Recorded by FDA as BARUQI LTD
As of October 26, 2026, Baruqi Ltd is not on any FDA import alert in SupplierRadar's records; FDA refused 3 of its shipment lines on December 8, 2020, most often for required information not prominent (COLORLABEL).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Plum, dried or paste · COLORLABEL
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Baruqi Ltd
3 records, newest first. Each line links to the FDA page it came from.
2020
- Import refusalSource
Refused, 3 lines in one entry: Plum, dried or paste; Apricot, dried or pasteCOLORLABELEntry BQL-0077694-6Show 3 linesHide lines
- Refused, Plum, dried or pasteCOLORLABELEntry BQL-0077694-6Source
- Refused, Apricot, dried or pasteCOLORLABELEntry BQL-0077694-6Source
- Refused, Plum, dried or pasteCOLORLABELEntry BQL-0077694-6Source
Refusal charges, in plain English
- COLORLABEL3 refused lines
Required information not prominent
Information required on the label appeared not to be placed prominently enough, or in such terms, to be read and understood by an ordinary consumer.
Questions about Baruqi Ltd
- Is Baruqi Ltd on an FDA import alert?
- No listing for Baruqi Ltd appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Georgia page.
- Has FDA refused shipments from Baruqi Ltd?
- Yes. FDA refused 3 shipment lines from Baruqi Ltd on December 8, 2020. The most recent, on December 8, 2020, was plum, dried or paste, charged as COLORLABEL (required information not prominent).
- Why did FDA refuse Baruqi Ltd's shipments?
- The most frequent charge is COLORLABEL (required information not prominent, 3 lines).
- What is Baruqi Ltd's FEI number?
- Baruqi Ltd's FDA Establishment Identifier (FEI) is 3013960831.
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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.