Adroit Overseas Ent Ltd
FDA import alert and refusal historySurrey, CanadaFEI 3022216058
Recorded by FDA as ADROIT OVERSEAS ENT LTD
As of October 26, 2026, Adroit Overseas Ent Ltd is not on any FDA import alert in SupplierRadar's records; FDA refused 3 of its shipment lines on May 24, 2023, most often for importer not in compliance with fsvp (FSVP VIO).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Peas · FSVP VIO
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Adroit Overseas Ent Ltd
3 records, newest first. Each line links to the FDA page it came from.
2023
- Import refusalSource
Refused, 3 lines in one entry: Peas; Garbanzo bean, dried or paste and 1 moreFSVP VIOEntry 572-6352634-5Show 3 linesHide lines
Refusal charges, in plain English
- FSVP VIO3 refused lines
Importer not in compliance with FSVP
The importer of record appeared not to be in compliance with the Foreign Supplier Verification Program requirements of section 805 of the FD&C Act. The charge concerns the importer's program, not a test result on the food.
Questions about Adroit Overseas Ent Ltd
- Is Adroit Overseas Ent Ltd on an FDA import alert?
- No listing for Adroit Overseas Ent Ltd appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Canada page.
- Has FDA refused shipments from Adroit Overseas Ent Ltd?
- Yes. FDA refused 3 shipment lines from Adroit Overseas Ent Ltd on May 24, 2023. The most recent, on May 24, 2023, was peas, charged as FSVP VIO (importer not in compliance with fsvp).
- Why did FDA refuse Adroit Overseas Ent Ltd's shipments?
- The most frequent charge is FSVP VIO (importer not in compliance with fsvp, 3 lines).
- What is Adroit Overseas Ent Ltd's FEI number?
- Adroit Overseas Ent Ltd's FDA Establishment Identifier (FEI) is 3022216058.
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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.