Glaxo Smith Kline
FDA import alert and refusal historyPunjab, IndiaFEI 3014289384
Recorded by FDA as GLAXO SMITH KLINE
As of October 26, 2026, Glaxo Smith Kline is not on any FDA import alert in SupplierRadar's records; FDA refused 2 of its shipment lines between August 10, 2018 and July 17, 2019, most often for nutrition information missing from label (NUTRIT LBL).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Malt beverages, n.e.c. · NUTRIT LBL
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Glaxo Smith Kline
2 records, newest first. Each line links to the FDA page it came from.
2019
- Import refusalRefused, Malt beverages, n.e.c.NUTRIT LBLEntry WD8-0062786-7Source
2018
- Import refusalRefused, Foods with supplemental nutrients added, with or without artifical sweetnersNUTRIT LBLEntry KM6-3514116-1Source
Refusal charges, in plain English
- NUTRIT LBL2 refused lines
Nutrition information missing from label
The label or labeling appeared not to carry the nutrition information that U.S. law requires for the food.
Questions about Glaxo Smith Kline
- Is Glaxo Smith Kline on an FDA import alert?
- No listing for Glaxo Smith Kline 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 Glaxo Smith Kline?
- Yes. FDA refused 2 shipment lines from Glaxo Smith Kline between August 10, 2018 and July 17, 2019. The most recent, on July 17, 2019, was malt beverages, n.e.c., charged as NUTRIT LBL (nutrition information missing from label).
- Why did FDA refuse Glaxo Smith Kline's shipments?
- The most frequent charge is NUTRIT LBL (nutrition information missing from label, 2 lines).
- What is Glaxo Smith Kline's FEI number?
- Glaxo Smith Kline's FDA Establishment Identifier (FEI) is 3014289384.
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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.