Munoz
FDA import alert and refusal historyAlmeria, SpainFEI 3004910267
As of October 25, 2026, Munoz (Almeria, Spain) is on the red list of FDA Import Alert 99-05 (Raw agricultural products: pesticides) for pepper, sweet (fruit used as vegetable), raw, fresh, ambient; pepper, sweet (fruit used as vegetable), raw, fresh, refrigerated, 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 99-05 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Munoz
1 record, newest first. Each line links to the FDA page it came from.
2009
- Import alert listingListed on Import Alert 99-05red listPepper, Sweet (Fruit Used as Vegetable), Raw, Fresh, Ambient; Pepper, Sweet (Fruit Used as Vegetable), Raw, Fresh, RefrigeratedSource
Questions about Munoz
- Is Munoz on an FDA import alert?
- Yes. As of October 25, 2026, Munoz is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for pepper, sweet (fruit used as vegetable), raw, fresh, ambient; pepper, sweet (fruit used as vegetable), raw, fresh, refrigerated; FDA published the listing on September 16, 2009.
- Has FDA refused shipments from Munoz?
- No FDA import refusals for Munoz appear in FDA's refusal data since October 2016, as of October 25, 2026.
- What is Munoz's FEI number?
- Munoz's FDA Establishment Identifier (FEI) is 3004910267.
- Can shipments from Munoz still enter the U.S.?
- Shipments of pepper, sweet (fruit used as vegetable), raw, fresh, ambient; pepper, sweet (fruit used as vegetable), raw, fresh, refrigerated from Munoz can be detained without physical examination under Import Alert 99-05; 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.