Jugos Concentrados Sa Jucosa
FDA import alert and refusal historySan Fernando, ChileFEI 1000169663
As of October 26, 2026, Jugos Concentrados Sa Jucosa (San Fernando, Chile) is on the red list of FDA Import Alert 99-08 (Processed human and animal foods: pesticides) for blackberry juice, berry juice or concentrates; blackberry syrup concentrate; blackberry syrup concentrate, published by FDA on September 16, 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 99-08 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Jugos Concentrados Sa Jucosa
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 99-08red listBlackberry Juice, Berry Juice or Concentrates; blackberry syrup concentrate; Blackberry syrup concentrateSource
Questions about Jugos Concentrados Sa Jucosa
- Is Jugos Concentrados Sa Jucosa on an FDA import alert?
- Yes. As of October 26, 2026, Jugos Concentrados Sa Jucosa is on the red list of FDA Import Alert 99-08, “Processed human and animal foods: pesticides”, for blackberry juice, berry juice or concentrates; blackberry syrup concentrate; blackberry syrup concentrate; FDA published the listing on September 16, 2009.
- Has FDA refused shipments from Jugos Concentrados Sa Jucosa?
- No FDA import refusals for Jugos Concentrados Sa Jucosa appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Jugos Concentrados Sa Jucosa's FEI number?
- Jugos Concentrados Sa Jucosa's FDA Establishment Identifier (FEI) is 1000169663.
- Can shipments from Jugos Concentrados Sa Jucosa still enter the U.S.?
- Shipments of blackberry juice, berry juice or concentrates; blackberry syrup concentrate; blackberry syrup concentrate from Jugos Concentrados Sa Jucosa can be detained without physical examination under Import Alert 99-08; 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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