Kay Bee Exports
FDA import alert and refusal historyAhmednagar, IndiaFEI 3008322685
As of October 25, 2026, Kay Bee Exports (Ahmednagar, India) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for mango, published by FDA on May 23, 2022, and has no FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 99-05 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- Classified VAI (Voluntary Action Indicated)
Every FDA record for Kay Bee Exports
2 records, newest first. Each line links to the FDA page it came from.
2022
- Import alert listingListed on Import Alert 99-05red listMangoSource
2012
- InspectionInspection classified VAI (Voluntary Action Indicated)Foodborne Biological HazardsSource
Questions about Kay Bee Exports
- Is Kay Bee Exports on an FDA import alert?
- Yes. As of October 25, 2026, Kay Bee Exports is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for mango; FDA published the listing on May 23, 2022.
- Has FDA refused shipments from Kay Bee Exports?
- No FDA import refusals for Kay Bee Exports appear in FDA's refusal data since October 2016, as of October 25, 2026.
- When was Kay Bee Exports last inspected by FDA?
- FDA's most recent inspection of Kay Bee Exports with a final classification is dated January 31, 2012 and was classified VAI (Voluntary Action Indicated).
- What is Kay Bee Exports's FEI number?
- Kay Bee Exports's FDA Establishment Identifier (FEI) is 3008322685.
- Can shipments from Kay Bee Exports still enter the U.S.?
- Shipments of mango from Kay Bee Exports can be detained without physical examination under Import Alert 99-05; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).
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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.