Industria Procesadora De Guatemala Sa Niasa
FDA import alert and refusal historyGuatemala, GuatemalaFEI 3009054952
As of October 26, 2026, Industria Procesadora De Guatemala Sa Niasa (Guatemala, Guatemala) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for assorted hard candy lollipops/chewing gum hard candy various flavors, published by FDA on October 20, 2011, 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 Industria Procesadora De Guatemala Sa Niasa
1 record, newest first. Each line links to the FDA page it came from.
2011
- Import alert listingListed on Import Alert 45-02red listAssorted Hard Candy Lollipops/chewing gum hard candy various flavorsSource
Questions about Industria Procesadora De Guatemala Sa Niasa
- Is Industria Procesadora De Guatemala Sa Niasa on an FDA import alert?
- Yes. As of October 26, 2026, Industria Procesadora De Guatemala Sa Niasa is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for assorted hard candy lollipops/chewing gum hard candy various flavors; FDA published the listing on October 20, 2011.
- Has FDA refused shipments from Industria Procesadora De Guatemala Sa Niasa?
- No FDA import refusals for Industria Procesadora De Guatemala Sa Niasa appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Industria Procesadora De Guatemala Sa Niasa's FEI number?
- Industria Procesadora De Guatemala Sa Niasa's FDA Establishment Identifier (FEI) is 3009054952.
- Can shipments from Industria Procesadora De Guatemala Sa Niasa still enter the U.S.?
- Shipments of assorted hard candy lollipops/chewing gum hard candy various flavors from Industria Procesadora De Guatemala Sa Niasa 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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