Ana Maria Moreira De Aquino
FDA import alert and refusal historyVinhedo, BrazilFEI 3012302027
As of October 26, 2026, Ana Maria Moreira De Aquino is not on any FDA import alert in SupplierRadar's records; FDA refused 6 of its shipment lines between May 14, 2018 and February 21, 2025, most often for processor not registered for canned or acidified foods (NEEDS FCE).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Pepper, black, ground, cracked (spice) · SALMONELLA
- Last warning letter
- None found
- Last inspection
- Classified VAI (Voluntary Action Indicated)
Every FDA record for Ana Maria Moreira De Aquino
7 records, newest first. Each line links to the FDA page it came from.
2025
- Import refusalRefused, Pepper, black, ground, cracked (spice)SALMONELLAEntry DP4-3851687-5Source
2023
- InspectionInspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
2019
- Import refusalSource
Refused, 3 lines in one entry: Subtropical fruit flavored imitation fruit; Pepper, sweet (fruit used as vegetable) and 1 moreNEEDS FCEEntry DP4-8259084-2Show 3 linesHide lines
2018
- Import refusalSource
Refused, 2 lines in one entry: Subtropical fruit flavored imitation fruit; Chili sauceNO PROCESSEntry DP4-8190899-5Show 2 linesHide lines
- Refused, Subtropical fruit flavored imitation fruitNO PROCESSEntry DP4-8190899-5Source
- Refused, Chili sauceNO PROCESSEntry DP4-8190899-5Source
Refusal charges, in plain English
- NEEDS FCE3 refused lines
Processor not registered for canned or acidified foods
The manufacturer appeared not to be registered with FDA as a low-acid canned food or acidified food processor, as 21 CFR 108.25 and 108.35 require.
- NO PROCESS2 refused lines
No scheduled process filed
The manufacturer appeared not to have filed a scheduled process with FDA, which 21 CFR Part 108 requires for low-acid canned and acidified foods, so the product is treated as made under insanitary conditions.
- SALMONELLA1 refused line
Salmonella
The product appeared to contain Salmonella, which the law treats as a poisonous and deleterious substance that may make food injurious to health.
Questions about Ana Maria Moreira De Aquino
- Is Ana Maria Moreira De Aquino on an FDA import alert?
- No listing for Ana Maria Moreira De Aquino appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Brazil page.
- Has FDA refused shipments from Ana Maria Moreira De Aquino?
- Yes. FDA refused 6 shipment lines from Ana Maria Moreira De Aquino between May 14, 2018 and February 21, 2025. The most recent, on February 21, 2025, was pepper, black, ground, cracked (spice), charged as SALMONELLA (salmonella).
- Why did FDA refuse Ana Maria Moreira De Aquino's shipments?
- The most frequent charges are NEEDS FCE (processor not registered for canned or acidified foods, 3 lines) and NO PROCESS (no scheduled process filed, 2 lines).
- When was Ana Maria Moreira De Aquino last inspected by FDA?
- FDA's most recent inspection of Ana Maria Moreira De Aquino with a final classification is dated July 13, 2023 and was classified VAI (Voluntary Action Indicated).
- What is Ana Maria Moreira De Aquino's FEI number?
- Ana Maria Moreira De Aquino's FDA Establishment Identifier (FEI) is 3012302027.
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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.