Brand Agency London
FDA import alert and refusal historyGreenhithe, United KingdomFEI 3012703079
Recorded by FDA as BRAND AGENCY LONDON
As of October 26, 2026, Brand Agency London is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on November 8, 2022, most often for color additive unsafe under section 721 (UNSAFE COL).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Cert. colors for use in cosmetics only, n.e.c. · UNSAFE COL
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Brand Agency London
1 record, newest first. Each line links to the FDA page it came from.
2022
- Import refusalRefused, Cert. colors for use in cosmetics only, n.e.c.UNSAFE COLEntry 799-1434241-5Source
Refusal charges, in plain English
- UNSAFE COL1 refused line
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.
Questions about Brand Agency London
- Is Brand Agency London on an FDA import alert?
- No listing for Brand Agency London appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the United Kingdom page.
- Has FDA refused shipments from Brand Agency London?
- Yes. FDA refused 1 shipment line from Brand Agency London on November 8, 2022. The most recent, on November 8, 2022, was cert. colors for use in cosmetics only, n.e.c., charged as UNSAFE COL (color additive unsafe under section 721).
- Why did FDA refuse Brand Agency London's shipments?
- The most frequent charge is UNSAFE COL (color additive unsafe under section 721, 1 line).
- What is Brand Agency London's FEI number?
- Brand Agency London's FDA Establishment Identifier (FEI) is 3012703079.
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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.