Coca Cola Bottles Philippines. Inc.
FDA import alert and refusal historyMandaluyong City, PhilippinesFEI 3004673998
As of October 26, 2026, Coca Cola Bottles Philippines. Inc. (Mandaluyong City, Philippines) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for soft drink, subtropical or tropical fruit flavored, carbonated, 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
- None on record
Every FDA record for Coca Cola Bottles Philippines. Inc.
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 45-02red listSoft Drink, Subtropical or Tropical Fruit Flavored, CarbonatedSource
Questions about Coca Cola Bottles Philippines. Inc.
- Is Coca Cola Bottles Philippines. Inc. on an FDA import alert?
- Yes. As of October 26, 2026, Coca Cola Bottles Philippines. Inc. is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for soft drink, subtropical or tropical fruit flavored, carbonated; FDA published the listing on September 18, 2009.
- Has FDA refused shipments from Coca Cola Bottles Philippines. Inc.?
- No FDA import refusals for Coca Cola Bottles Philippines. Inc. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Coca Cola Bottles Philippines. Inc.'s FEI number?
- Coca Cola Bottles Philippines. Inc.'s FDA Establishment Identifier (FEI) is 3004673998.
- Can shipments from Coca Cola Bottles Philippines. Inc. still enter the U.S.?
- Shipments of soft drink, subtropical or tropical fruit flavored, carbonated from Coca Cola Bottles Philippines. 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.