Laura's Food Products Corporation
FDA import alert and refusal historyAngono, PhilippinesFEI 3004274237
As of October 26, 2026, Laura's Food Products Corporation (Angono, Philippines) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for ogoy ogoy, published by FDA on September 18, 2009, 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 45-02 · 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 Laura's Food Products Corporation
2 records, newest first. Each line links to the FDA page it came from.
2013
- InspectionInspection classified VAI (Voluntary Action Indicated)Foodborne Biological HazardsSource
2009
- Import alert listingListed on Import Alert 45-02red listogoy ogoySource
Questions about Laura's Food Products Corporation
- Is Laura's Food Products Corporation on an FDA import alert?
- Yes. As of October 26, 2026, Laura's Food Products Corporation is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for ogoy ogoy; FDA published the listing on September 18, 2009.
- Has FDA refused shipments from Laura's Food Products Corporation?
- No FDA import refusals for Laura's Food Products Corporation appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Laura's Food Products Corporation last inspected by FDA?
- FDA's most recent inspection of Laura's Food Products Corporation with a final classification is dated May 23, 2013 and was classified VAI (Voluntary Action Indicated).
- What is Laura's Food Products Corporation's FEI number?
- Laura's Food Products Corporation's FDA Establishment Identifier (FEI) is 3004274237.
- Can shipments from Laura's Food Products Corporation still enter the U.S.?
- Shipments of ogoy ogoy from Laura's Food Products Corporation can be detained without physical examination under Import Alert 45-02; 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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