Felicisimo Martinez & Co., Inc.
FDA import alert and refusal historyAntipolo City, PhilippinesFEI 3004248803
As of October 26, 2026, Felicisimo Martinez & Co., Inc. (Antipolo City, Philippines) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for egg cracklet, 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 Felicisimo Martinez & Co., Inc.
2 records, newest first. Each line links to the FDA page it came from.
2017
- InspectionInspection classified VAI (Voluntary Action Indicated)Foodborne Biological HazardsSource
2009
- Import alert listingListed on Import Alert 45-02red listEgg CrackletSource
Questions about Felicisimo Martinez & Co., Inc.
- Is Felicisimo Martinez & Co., Inc. on an FDA import alert?
- Yes. As of October 26, 2026, Felicisimo Martinez & Co., Inc. is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for egg cracklet; FDA published the listing on September 18, 2009.
- Has FDA refused shipments from Felicisimo Martinez & Co., Inc.?
- No FDA import refusals for Felicisimo Martinez & Co., Inc. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Felicisimo Martinez & Co., Inc. last inspected by FDA?
- FDA's most recent inspection of Felicisimo Martinez & Co., Inc. with a final classification is dated October 21, 2017 and was classified VAI (Voluntary Action Indicated).
- What is Felicisimo Martinez & Co., Inc.'s FEI number?
- Felicisimo Martinez & Co., Inc.'s FDA Establishment Identifier (FEI) is 3004248803.
- Can shipments from Felicisimo Martinez & Co., Inc. still enter the U.S.?
- Shipments of egg cracklet from Felicisimo Martinez & Co., Inc. 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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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.