C.I. Procepack Ltda
FDA import alert and refusal historySantafe De Bogota, ColombiaFEI 3003112187
As of October 26, 2026, C.I. Procepack Ltda (Santafe De Bogota, Colombia) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for soft drink, citrus fruit flavored, carbonated; soft drink, mixed fruit flavored, carbonated; soft drink, other 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 C.I. Procepack Ltda
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, Citrus Fruit Flavored, Carbonated; Soft Drink, Mixed Fruit Flavored, Carbonated; Soft Drink, Other Fruit Flavored, CarbonatedSource
Questions about C.I. Procepack Ltda
- Is C.I. Procepack Ltda on an FDA import alert?
- Yes. As of October 26, 2026, C.I. Procepack Ltda is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for soft drink, citrus fruit flavored, carbonated; soft drink, mixed fruit flavored, carbonated; soft drink, other fruit flavored, carbonated; FDA published the listing on September 18, 2009.
- Has FDA refused shipments from C.I. Procepack Ltda?
- No FDA import refusals for C.I. Procepack Ltda appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is C.I. Procepack Ltda's FEI number?
- C.I. Procepack Ltda's FDA Establishment Identifier (FEI) is 3003112187.
- Can shipments from C.I. Procepack Ltda still enter the U.S.?
- Shipments of soft drink, citrus fruit flavored, carbonated; soft drink, mixed fruit flavored, carbonated; soft drink, other fruit flavored, carbonated from C.I. Procepack Ltda 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.