Naturefield Company Limited
FDA import alert and refusal historyKingston, JamaicaFEI 3013178862
As of October 27, 2026, Naturefield Company Limited (Kingston, Jamaica) is on the red list of FDA Import Alert 20-07 (Juice from processors not in compliance with juice HACCP) for 100% coconut water, published by FDA on January 4, 2018, 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 20-07 · 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 Naturefield Company Limited
2 records, newest first. Each line links to the FDA page it came from.
2018
- Import alert listingListed on Import Alert 20-07red list100% Coconut WaterSource
2017
- InspectionInspection classified NAI (No Action Indicated)Foodborne Biological HazardsSource
Questions about Naturefield Company Limited
- Is Naturefield Company Limited on an FDA import alert?
- Yes. As of October 27, 2026, Naturefield Company Limited is on the red list of FDA Import Alert 20-07, “Juice from processors not in compliance with juice HACCP”, for 100% coconut water; FDA published the listing on January 4, 2018.
- Has FDA refused shipments from Naturefield Company Limited?
- No FDA import refusals for Naturefield Company Limited appear in FDA's refusal data since October 2016, as of October 27, 2026.
- When was Naturefield Company Limited last inspected by FDA?
- FDA's most recent inspection of Naturefield Company Limited with a final classification is dated May 29, 2017 and was classified NAI (No Action Indicated).
- What is Naturefield Company Limited's FEI number?
- Naturefield Company Limited's FDA Establishment Identifier (FEI) is 3013178862.
- Can shipments from Naturefield Company Limited still enter the U.S.?
- Shipments of 100% coconut water from Naturefield Company Limited can be detained without physical examination under Import Alert 20-07; 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.