Dairboard Holdings Ltd
FDA import alert and refusal historyHarare, South AfricaFEI 3013793136
Recorded by FDA as DAIRBOARD HOLDINGS LTD
As of October 26, 2026, Dairboard Holdings Ltd is not on any FDA import alert in SupplierRadar's records; FDA refused 3 of its shipment lines on February 1, 2018, most often for fair packaging and labeling act (LABELING).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Noncarbonated soft drink, n.e.c. · LABELING
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Dairboard Holdings Ltd
3 records, newest first. Each line links to the FDA page it came from.
2018
- Import refusalSource
Refused, 3 lines in one entry: Noncarbonated soft drink, n.e.c.; Cereal preparations not elsewhere mentioned, n.e.c.LABELINGEntry 9DH-0016116-1Show 3 linesHide lines
Refusal charges, in plain English
- LABELING3 refused lines
Fair Packaging and Labeling Act
The package appeared not to meet the Fair Packaging and Labeling Act because of the placement, form, or contents of a required label statement.
Questions about Dairboard Holdings Ltd
- Is Dairboard Holdings Ltd on an FDA import alert?
- No listing for Dairboard Holdings Ltd 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 Dairboard Holdings Ltd?
- Yes. FDA refused 3 shipment lines from Dairboard Holdings Ltd on February 1, 2018. The most recent, on February 1, 2018, was noncarbonated soft drink, n.e.c., charged as LABELING (fair packaging and labeling act).
- Why did FDA refuse Dairboard Holdings Ltd's shipments?
- The most frequent charge is LABELING (fair packaging and labeling act, 3 lines).
- What is Dairboard Holdings Ltd's FEI number?
- Dairboard Holdings Ltd's FDA Establishment Identifier (FEI) is 3013793136.
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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.