La Purisima Sa. De Cv.
FDA import alert and refusal historyTijuana, MexicoFEI 3004558254
As of October 26, 2026, La Purisima Sa. De Cv. (Tijuana, Mexico) is on the red list of FDA Import Alert 45-02 (Foods with illegal or undeclared colors) for soft drink, vine fruit flavored, noncarbonated; noncarbonated soft drink, n.e.c.; soft drinks and waters not mentioned elsewhere, n.e.c., 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 La Purisima Sa. De Cv.
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, Vine Fruit Flavored, Noncarbonated; Noncarbonated Soft Drink, N.E.C.; Soft Drinks and Waters Not Mentioned Elsewhere, N.E.C.Source
Questions about La Purisima Sa. De Cv.
- Is La Purisima Sa. De Cv. on an FDA import alert?
- Yes. As of October 26, 2026, La Purisima Sa. De Cv. is on the red list of FDA Import Alert 45-02, “Foods with illegal or undeclared colors”, for soft drink, vine fruit flavored, noncarbonated; noncarbonated soft drink, n.e.c.; soft drinks and waters not mentioned elsewhere, n.e.c.; FDA published the listing on September 18, 2009.
- Has FDA refused shipments from La Purisima Sa. De Cv.?
- No FDA import refusals for La Purisima Sa. De Cv. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is La Purisima Sa. De Cv.'s FEI number?
- La Purisima Sa. De Cv.'s FDA Establishment Identifier (FEI) is 3004558254.
- Can shipments from La Purisima Sa. De Cv. still enter the U.S.?
- Shipments of soft drink, vine fruit flavored, noncarbonated; noncarbonated soft drink, n.e.c.; soft drinks and waters not mentioned elsewhere, n.e.c. from La Purisima Sa. De Cv. 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.