Shahadat Ramlakan Ltd
FDA import alert and refusal historyRio Claro, Trinidad and TobagoFEI 3010132701
Recorded by FDA as SHAHADAT RAMLAKAN LTD
As of October 26, 2026, Shahadat Ramlakan Ltd (Rio Claro, Trinidad and Tobago) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for peppers, published by FDA on May 6, 2014, is also listed on Import Alert 99-23 (red list), 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 99-05 · red listIA 99-23 · 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 Shahadat Ramlakan Ltd
3 records, newest first. Each line links to the FDA page it came from.
2014
- Import alert listingListed on Import Alert 99-05red listPeppersSource
2013
- InspectionInspection classified NAI (No Action Indicated)Foodborne Biological HazardsSource
2010
- Import alert listingListed on Import Alert 99-23red listCoriander (Cilantro)Source
Questions about Shahadat Ramlakan Ltd
- Is Shahadat Ramlakan Ltd on an FDA import alert?
- Yes. As of October 26, 2026, Shahadat Ramlakan Ltd is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for peppers; FDA published the listing on May 6, 2014.
- Has FDA refused shipments from Shahadat Ramlakan Ltd?
- No FDA import refusals for Shahadat Ramlakan Ltd appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Shahadat Ramlakan Ltd last inspected by FDA?
- FDA's most recent inspection of Shahadat Ramlakan Ltd with a final classification is dated November 20, 2013 and was classified NAI (No Action Indicated).
- What is Shahadat Ramlakan Ltd's FEI number?
- Shahadat Ramlakan Ltd's FDA Establishment Identifier (FEI) is 3010132701.
- Can shipments from Shahadat Ramlakan Ltd still enter the U.S.?
- Shipments of peppers from Shahadat Ramlakan Ltd can be detained without physical examination under Import Alert 99-05; 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.