Francisco Garcia Garcia
FDA import alert and refusal historyArchena, SpainFEI 11523
As of October 26, 2026, Francisco Garcia Garcia (Archena, Spain) is on the red list of FDA Import Alert 99-36 (Low-acid canned/acidified foods: process information) for tuna in tomato sauce; artichokes (hearts and bottoms; whole; halved and quartered) in brine, published by FDA on June 3, 2014, is also listed on Import Alert 99-38 (red list), 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 99-36 · red listIA 99-38 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Francisco Garcia Garcia
2 records, newest first. Each line links to the FDA page it came from.
2014
- Import alert listingListed on Import Alert 99-36red listTuna in tomato sauce; artichokes (hearts and bottoms; whole; halved and quartered) in brineSource
- Import alert listingListed on Import Alert 99-38red listPimientos (whole; striped; diced and broken)Source
Questions about Francisco Garcia Garcia
- Is Francisco Garcia Garcia on an FDA import alert?
- Yes. As of October 26, 2026, Francisco Garcia Garcia is on the red list of FDA Import Alert 99-36, “Low-acid canned/acidified foods: process information”, for tuna in tomato sauce; artichokes (hearts and bottoms; whole; halved and quartered) in brine; FDA published the listing on June 3, 2014.
- Has FDA refused shipments from Francisco Garcia Garcia?
- No FDA import refusals for Francisco Garcia Garcia appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Francisco Garcia Garcia's FEI number?
- Francisco Garcia Garcia's FDA Establishment Identifier (FEI) is 11523.
- Can shipments from Francisco Garcia Garcia still enter the U.S.?
- Shipments of tuna in tomato sauce; artichokes (hearts and bottoms; whole; halved and quartered) in brine from Francisco Garcia Garcia can be detained without physical examination under Import Alert 99-36; 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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