Ladiva Enterprise
FDA import alert and refusal historyPrampram, GhanaFEI 3013241775
As of October 26, 2026, Ladiva Enterprise (Prampram, Ghana) is on the red list of FDA Import Alert 16-81 (Seafood products: Salmonella) for tilapia; hot smoked, published by FDA on May 15, 2015, 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 16-81 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- Classified VAI (Voluntary Action Indicated)
Every FDA record for Ladiva Enterprise
2 records, newest first. Each line links to the FDA page it came from.
2019
- InspectionInspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
2015
- Import alert listingListed on Import Alert 16-81red listTilapia; Hot SmokedSource
Questions about Ladiva Enterprise
- Is Ladiva Enterprise on an FDA import alert?
- Yes. As of October 26, 2026, Ladiva Enterprise is on the red list of FDA Import Alert 16-81, “Seafood products: Salmonella”, for tilapia; hot smoked; FDA published the listing on May 15, 2015.
- Has FDA refused shipments from Ladiva Enterprise?
- No FDA import refusals for Ladiva Enterprise appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Ladiva Enterprise last inspected by FDA?
- FDA's most recent inspection of Ladiva Enterprise with a final classification is dated December 13, 2019 and was classified VAI (Voluntary Action Indicated).
- What is Ladiva Enterprise's FEI number?
- Ladiva Enterprise's FDA Establishment Identifier (FEI) is 3013241775.
- Can shipments from Ladiva Enterprise still enter the U.S.?
- Shipments of tilapia; hot smoked from Ladiva Enterprise can be detained without physical examination under Import Alert 16-81; 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.