Can and Kaa Limited
FDA import alert and refusal historyAccra, GhanaFEI 3011329528
As of October 26, 2026, Can and Kaa Limited is not on any FDA import alert in SupplierRadar's records; FDA refused 3 of its shipment lines on July 21, 2021, 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
- Fish, n.e.c. · LABELING
- Last warning letter
- None found
- Last inspection
- Classified VAI (Voluntary Action Indicated)
Every FDA record for Can and Kaa Limited
4 records, newest first. Each line links to the FDA page it came from.
2021
2018
- InspectionInspection classified VAI (Voluntary Action Indicated)Foodborne Biological HazardsSource
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 Can and Kaa Limited
- Is Can and Kaa Limited on an FDA import alert?
- No listing for Can and Kaa Limited appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Ghana page.
- Has FDA refused shipments from Can and Kaa Limited?
- Yes. FDA refused 3 shipment lines from Can and Kaa Limited on July 21, 2021. The most recent, on July 21, 2021, was fish, n.e.c., charged as LABELING (fair packaging and labeling act).
- Why did FDA refuse Can and Kaa Limited's shipments?
- The most frequent charge is LABELING (fair packaging and labeling act, 3 lines).
- When was Can and Kaa Limited last inspected by FDA?
- FDA's most recent inspection of Can and Kaa Limited with a final classification is dated May 16, 2018 and was classified VAI (Voluntary Action Indicated).
- What is Can and Kaa Limited's FEI number?
- Can and Kaa Limited's FDA Establishment Identifier (FEI) is 3011329528.
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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.