Miguel Rafael Gabriel Food Product
FDA import alert and refusal historyCavite City, PhilippinesFEI 3010040158
As of October 26, 2026, Miguel Rafael Gabriel Food Product (Cavite City, Philippines) is on the red list of FDA Import Alert 99-19 (Food products: Salmonella) for malou's - biscocho iloilo - cookie, published by FDA on September 3, 2020, 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 99-19 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Miguel Rafael Gabriel Food Product
1 record, newest first. Each line links to the FDA page it came from.
2020
- Import alert listingListed on Import Alert 99-19red listMalou's - biscocho iloilo - cookieSource
Questions about Miguel Rafael Gabriel Food Product
- Is Miguel Rafael Gabriel Food Product on an FDA import alert?
- Yes. As of October 26, 2026, Miguel Rafael Gabriel Food Product is on the red list of FDA Import Alert 99-19, “Food products: Salmonella”, for malou's - biscocho iloilo - cookie; FDA published the listing on September 3, 2020.
- Has FDA refused shipments from Miguel Rafael Gabriel Food Product?
- No FDA import refusals for Miguel Rafael Gabriel Food Product appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Miguel Rafael Gabriel Food Product's FEI number?
- Miguel Rafael Gabriel Food Product's FDA Establishment Identifier (FEI) is 3010040158.
- Can shipments from Miguel Rafael Gabriel Food Product still enter the U.S.?
- Shipments of malou's - biscocho iloilo - cookie from Miguel Rafael Gabriel Food Product can be detained without physical examination under Import Alert 99-19; 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.