M.N. International
FDA import alert and refusal historyNorth Agarabad, BangladeshFEI 3011297853
As of October 26, 2026, M.N. International is not on any FDA import alert in SupplierRadar's records; FDA refused 1 of its shipment line on November 8, 2023, most often for poisonous or deleterious substance (ordinarily injurious) (POISONORD).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Betel nut, in shell · POISONORD
- Last warning letter
- None found
- Last inspection
- Classified VAI (Voluntary Action Indicated)
Every FDA record for M.N. International
2 records, newest first. Each line links to the FDA page it came from.
Refusal charges, in plain English
- POISONORD1 refused line
Poisonous or deleterious substance (ordinarily injurious)
The product appeared to contain a poisonous or deleterious substance in a form or amount that would ordinarily render it injurious to health.
Questions about M.N. International
- Is M.N. International on an FDA import alert?
- No listing for M.N. International appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Bangladesh page.
- Has FDA refused shipments from M.N. International?
- Yes. FDA refused 1 shipment line from M.N. International on November 8, 2023. The most recent, on November 8, 2023, was betel nut, in shell, charged as POISONORD (poisonous or deleterious substance (ordinarily injurious)).
- Why did FDA refuse M.N. International's shipments?
- The most frequent charge is POISONORD (poisonous or deleterious substance (ordinarily injurious), 1 line).
- When was M.N. International last inspected by FDA?
- FDA's most recent inspection of M.N. International with a final classification is dated August 2, 2015 and was classified VAI (Voluntary Action Indicated).
- What is M.N. International's FEI number?
- M.N. International's FDA Establishment Identifier (FEI) is 3011297853.
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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.