Summer Fruit Inc (Factory), Marsman-Drysdale Group
FDA import alert and refusal historyCavite, PhilippinesFEI 1000209541
As of October 26, 2026, Summer Fruit Inc (Factory), Marsman-Drysdale Group (Cavite, Philippines) is on the red list of FDA Import Alert 99-53 (Foods: naturally occurring toxins) for guanabana, published by FDA on September 28, 2026, is also listed on Import Alert 31-03 (red list), 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 99-53 · red listIA 31-03 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Summer Fruit Inc (Factory), Marsman-Drysdale Group
2 records, newest first. Each line links to the FDA page it came from.
2026
- Import alert listingListed on Import Alert 99-53red listGuanabanaSource
2009
- Import alert listingListed on Import Alert 31-03red listGuanabanaSource
Questions about Summer Fruit Inc (Factory), Marsman-Drysdale Group
- Is Summer Fruit Inc (Factory), Marsman-Drysdale Group on an FDA import alert?
- Yes. As of October 26, 2026, Summer Fruit Inc (Factory), Marsman-Drysdale Group is on the red list of FDA Import Alert 99-53, “Foods: naturally occurring toxins”, for guanabana; FDA published the listing on September 28, 2026.
- Has FDA refused shipments from Summer Fruit Inc (Factory), Marsman-Drysdale Group?
- No FDA import refusals for Summer Fruit Inc (Factory), Marsman-Drysdale Group appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Summer Fruit Inc (Factory), Marsman-Drysdale Group's FEI number?
- Summer Fruit Inc (Factory), Marsman-Drysdale Group's FDA Establishment Identifier (FEI) is 1000209541.
- Can shipments from Summer Fruit Inc (Factory), Marsman-Drysdale Group still enter the U.S.?
- Shipments of guanabana from Summer Fruit Inc (Factory), Marsman-Drysdale Group can be detained without physical examination under Import Alert 99-53; 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.