Gsk Ltd
FDA import alert and refusal historyKarnataka, IndiaFEI 3048144362
Recorded by FDA as GSK LTD
As of October 26, 2026, Gsk Ltd is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on September 24, 2026, most often for product not listed with fda (NOT LISTED).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Vitamin b6 (pyridoxine) · NOT LISTED
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Gsk Ltd
1 record, newest first. Each line links to the FDA page it came from.
2026
- Import refusalRefused, Vitamin b6 (pyridoxine)NOT LISTEDUNAPPROVEDEntry 1FX-4852481-4Source
Refusal charges, in plain English
- NOT LISTED1 refused line
Product not listed with FDA
The product appeared to be a drug or device that is not included in the listing FDA requires under section 510(j) of the FD&C Act.
- UNAPPROVED1 refused line
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 Gsk Ltd
- Is Gsk Ltd on an FDA import alert?
- No listing for Gsk Ltd 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 Gsk Ltd?
- Yes. FDA refused 1 shipment line from Gsk Ltd on September 24, 2026. The most recent, on September 24, 2026, was vitamin b6 (pyridoxine), charged as NOT LISTED (product not listed with fda).
- Why did FDA refuse Gsk Ltd's shipments?
- The most frequent charges are NOT LISTED (product not listed with fda, 1 line) and UNAPPROVED (unapproved new drug, 1 line).
- What is Gsk Ltd's FEI number?
- Gsk Ltd's FDA Establishment Identifier (FEI) is 3048144362.
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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.