GELITA do Brasil Ltda.
FDA import alert and refusal historyCotia, BrazilFEI 3004278863
As of October 26, 2026, GELITA do Brasil Ltda. is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on July 31, 2018, most often for salmonella (SALMONELLA).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Stabilizers and thickeners (food additives for human use) · SALMONELLA
- Last warning letter
- None found
- Last inspection
- Classified NAI (No Action Indicated)
Every FDA record for GELITA do Brasil Ltda.
2 records, newest first. Each line links to the FDA page it came from.
2023
- InspectionInspection classified NAI (No Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
2018
- Import refusalRefused, Stabilizers and thickeners (food additives for human use)SALMONELLAEntry AF4-0849410-8Source
Refusal charges, in plain English
- 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 GELITA do Brasil Ltda.
- Is GELITA do Brasil Ltda. on an FDA import alert?
- No listing for GELITA do Brasil Ltda. 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 GELITA do Brasil Ltda.?
- Yes. FDA refused 1 shipment line from GELITA do Brasil Ltda. on July 31, 2018. The most recent, on July 31, 2018, was stabilizers and thickeners (food additives for human use), charged as SALMONELLA (salmonella).
- Why did FDA refuse GELITA do Brasil Ltda.'s shipments?
- The most frequent charge is SALMONELLA (salmonella, 1 line).
- When was GELITA do Brasil Ltda. last inspected by FDA?
- FDA's most recent inspection of GELITA do Brasil Ltda. with a final classification is dated July 7, 2023 and was classified NAI (No Action Indicated).
- What is GELITA do Brasil Ltda.'s FEI number?
- GELITA do Brasil Ltda.'s FDA Establishment Identifier (FEI) is 3004278863.
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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.