Fernando & Simoes, Lda
FDA import alert and refusal historyQuinta do Anjo, PortugalFEI 3010137911
Recorded by FDA as FERNANDO & SIMOES, LDA
As of October 26, 2026, Fernando & Simoes, Lda (Quinta do Anjo, Portugal) is on the red list of FDA Import Alert 99-43 (Ready-to-eat foods: insanitary conditions) for azeltao cheese, published by FDA on August 27, 2025, 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 99-43 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- Classified OAI (Official Action Indicated)
Every FDA record for Fernando & Simoes, Lda
2 records, newest first. Each line links to the FDA page it came from.
2025
- Import alert listingListed on Import Alert 99-43red listAzeltao CheeseSource
2014
- InspectionInspection classified OAI (Official Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
Questions about Fernando & Simoes, Lda
- Is Fernando & Simoes, Lda on an FDA import alert?
- Yes. As of October 26, 2026, Fernando & Simoes, Lda is on the red list of FDA Import Alert 99-43, “Ready-to-eat foods: insanitary conditions”, for azeltao cheese; FDA published the listing on August 27, 2025.
- Has FDA refused shipments from Fernando & Simoes, Lda?
- No FDA import refusals for Fernando & Simoes, Lda appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Fernando & Simoes, Lda last inspected by FDA?
- FDA's most recent inspection of Fernando & Simoes, Lda with a final classification is dated February 4, 2014 and was classified OAI (Official Action Indicated).
- What is Fernando & Simoes, Lda's FEI number?
- Fernando & Simoes, Lda's FDA Establishment Identifier (FEI) is 3010137911.
- Can shipments from Fernando & Simoes, Lda still enter the U.S.?
- Shipments of azeltao cheese from Fernando & Simoes, Lda can be detained without physical examination under Import Alert 99-43; 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.