Gurinder Kaur
FDA import alert and refusal historyHoshiarpur, IndiaFEI 3031437107
Recorded by FDA as GURINDER KAUR
As of October 26, 2026, Gurinder Kaur is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines on November 7, 2024, most often for unapproved new drug (UNAPPROVED).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c. · UNAPPROVED
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Gurinder Kaur
2 records, newest first. Each line links to the FDA page it came from.
2024
- Import refusalSource
Refused, 2 lines in one entry: Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.UNAPPROVEDEntry SCS-6850306-3Show 2 linesHide lines
- Refused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.UNAPPROVEDEntry SCS-6850306-3Source
- Refused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.UNAPPROVEDEntry SCS-6850306-3Source
Refusal charges, in plain English
- UNAPPROVED2 refused lines
Unapproved new drug
The product appeared to be a new drug within the meaning of section 201(p) of the FD&C Act without an approved New Drug Application. FDA can apply this charge to a food or supplement whose labeling presents it for drug uses.
Questions about Gurinder Kaur
- Is Gurinder Kaur on an FDA import alert?
- No listing for Gurinder Kaur appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the India page.
- Has FDA refused shipments from Gurinder Kaur?
- Yes. FDA refused 2 shipment lines from Gurinder Kaur on November 7, 2024. The most recent, on November 7, 2024, was vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c., charged as UNAPPROVED (unapproved new drug).
- Why did FDA refuse Gurinder Kaur's shipments?
- The most frequent charge is UNAPPROVED (unapproved new drug, 2 lines).
- What is Gurinder Kaur's FEI number?
- Gurinder Kaur's FDA Establishment Identifier (FEI) is 3031437107.
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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.