Botako Enterprise
FDA import alert and refusal historyAchimota, GhanaFEI 3014716879
Recorded by FDA as BOTAKO ENTERPRISE
As of October 25, 2026, Botako Enterprise (Achimota, Ghana) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for maggi shrimp seasoning, published by FDA on September 25, 2024, and has no FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 45-02 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- Classified NAI (No Action Indicated)
Every FDA record for Botako Enterprise
2 records, newest first. Each line links to the FDA page it came from.
2024
- Import alert listingListed on Import Alert 45-02red listMaggi Shrimp SeasoningSource
- InspectionInspection classified NAI (No Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
Questions about Botako Enterprise
- Is Botako Enterprise on an FDA import alert?
- Yes. As of October 25, 2026, Botako Enterprise is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for maggi shrimp seasoning; FDA published the listing on September 25, 2024.
- Has FDA refused shipments from Botako Enterprise?
- No FDA import refusals for Botako Enterprise appear in FDA's refusal data since October 2016, as of October 25, 2026.
- When was Botako Enterprise last inspected by FDA?
- FDA's most recent inspection of Botako Enterprise with a final classification is dated September 4, 2024 and was classified NAI (No Action Indicated).
- What is Botako Enterprise's FEI number?
- Botako Enterprise's FDA Establishment Identifier (FEI) is 3014716879.
- Can shipments from Botako Enterprise still enter the U.S.?
- Shipments of maggi shrimp seasoning from Botako Enterprise can be detained without physical examination under Import Alert 45-02; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).
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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.