Apex International
FDA import alert and refusal historySojat, IndiaFEI 3011281554
As of October 26, 2026, Apex International is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on March 17, 2020, most often for salmonella (SALMONELLA).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Fiber, n.e.c. · SALMONELLA
- Last warning letter
- None found
- Last inspection
- Classified VAI (Voluntary Action Indicated)
Every FDA record for Apex International
2 records, newest first. Each line links to the FDA page it came from.
2020
- Import refusalRefused, Fiber, n.e.c.SALMONELLAEntry E94-2010353-9Source
2012
- InspectionInspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and EconSource
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 Apex International
- Is Apex International on an FDA import alert?
- No listing for Apex International appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the India page.
- Has FDA refused shipments from Apex International?
- Yes. FDA refused 1 shipment line from Apex International on March 17, 2020. The most recent, on March 17, 2020, was fiber, n.e.c., charged as SALMONELLA (salmonella).
- Why did FDA refuse Apex International's shipments?
- The most frequent charge is SALMONELLA (salmonella, 1 line).
- When was Apex International last inspected by FDA?
- FDA's most recent inspection of Apex International with a final classification is dated May 11, 2012 and was classified VAI (Voluntary Action Indicated).
- What is Apex International's FEI number?
- Apex International's FDA Establishment Identifier (FEI) is 3011281554.
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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.