Is Golden Cape on an FDA import alert?

No listing for Golden Cape appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the South Africa page.

Has FDA refused shipments from Golden Cape?

Yes. FDA refused 1 shipment line from Golden Cape on March 16, 2017. The most recent, on March 16, 2017, was natural extract or flavor, n.e.c., charged as UNSAFE ADD (food additive unsafe under section 409).

Why did FDA refuse Golden Cape's shipments?

The most frequent charge is UNSAFE ADD (food additive unsafe under section 409, 1 line).

When was Golden Cape last inspected by FDA?

FDA's most recent inspection of Golden Cape with a final classification is dated March 22, 2018 and was classified NAI (No Action Indicated).

What is Golden Cape's FEI number?

Golden Cape's FDA Establishment Identifier (FEI) is 3010332745.

Golden Cape

FDA import alert and refusal historyDurbanville, South AfricaFEI 3010332745

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As of October 26, 2026, Golden Cape is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on March 16, 2017, most often for food additive unsafe under section 409 (UNSAFE ADD).

Data from FDA public records, last checked October 26, 2026. Request a correction

Current status

Import alerts: Not listed
Last import refusal: Mar 16, 2017Natural extract or flavor, n.e.c. · UNSAFE ADD
Last warning letter: None found
Last inspection: Mar 22, 2018Classified NAI (No Action Indicated)

Every FDA record for Golden Cape

2 records, newest first. Each line links to the FDA page it came from.

2018

Mar 22, 2018Inspection
Inspection classified NAI (No Action Indicated)Foodborne Biological Hazards
Source

2017

Mar 16, 2017Import refusal
Refused, Natural extract or flavor, n.e.c.UNSAFE ADDEntry 112-8234994-8
Source

Refusal charges, in plain English

UNSAFE ADD1 refused line
Food additive unsafe under section 409
The product appeared to contain a food additive that is unsafe within the meaning of section 409 of the FD&C Act, the section that governs which food additives may be used and under what conditions.

Questions about Golden Cape

Is Golden Cape on an FDA import alert?: No listing for Golden Cape appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the South Africa page.
Has FDA refused shipments from Golden Cape?: Yes. FDA refused 1 shipment line from Golden Cape on March 16, 2017. The most recent, on March 16, 2017, was natural extract or flavor, n.e.c., charged as UNSAFE ADD (food additive unsafe under section 409).
Why did FDA refuse Golden Cape's shipments?: The most frequent charge is UNSAFE ADD (food additive unsafe under section 409, 1 line).
When was Golden Cape last inspected by FDA?: FDA's most recent inspection of Golden Cape with a final classification is dated March 22, 2018 and was classified NAI (No Action Indicated).
What is Golden Cape's FEI number?: Golden Cape's FDA Establishment Identifier (FEI) is 3010332745.

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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.