LASCO Manufacturing Limited
FDA import alert and refusal historySpanish Town 1, JamaicaFEI 3014168320
As of October 26, 2026, LASCO Manufacturing Limited (Spanish Town 1, Jamaica) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for lasco strawberry syrup, published by FDA on January 7, 2014, 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 LASCO Manufacturing Limited
2 records, newest first. Each line links to the FDA page it came from.
2019
- InspectionInspection classified NAI (No Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
2014
- Import alert listingListed on Import Alert 45-02red listLasco Strawberry SyrupSource
Questions about LASCO Manufacturing Limited
- Is LASCO Manufacturing Limited on an FDA import alert?
- Yes. As of October 26, 2026, LASCO Manufacturing Limited is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for lasco strawberry syrup; FDA published the listing on January 7, 2014.
- Has FDA refused shipments from LASCO Manufacturing Limited?
- No FDA import refusals for LASCO Manufacturing Limited appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was LASCO Manufacturing Limited last inspected by FDA?
- FDA's most recent inspection of LASCO Manufacturing Limited with a final classification is dated July 11, 2019 and was classified NAI (No Action Indicated).
- What is LASCO Manufacturing Limited's FEI number?
- LASCO Manufacturing Limited's FDA Establishment Identifier (FEI) is 3014168320.
- Can shipments from LASCO Manufacturing Limited still enter the U.S.?
- Shipments of lasco strawberry syrup from LASCO Manufacturing Limited 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.