Cremeria Vero Interior Del Mercado Municipal
FDA import alert and refusal historyIguala, MexicoFEI 3003816149
As of October 26, 2026, Cremeria Vero Interior Del Mercado Municipal (Iguala, Mexico) is on the red list of FDA Import Alert 99-43 (Ready-to-eat foods: insanitary conditions) for cheese/cheese products, published by FDA on August 27, 2025, is also listed on Import Alert 12-10 (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 99-43 · red listIA 12-10 · red list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Cremeria Vero Interior Del Mercado Municipal
2 records, newest first. Each line links to the FDA page it came from.
2025
- Import alert listingListed on Import Alert 99-43red listCheese/Cheese ProductsSource
2009
- Import alert listingListed on Import Alert 12-10red listCheese/Cheese ProductsSource
Questions about Cremeria Vero Interior Del Mercado Municipal
- Is Cremeria Vero Interior Del Mercado Municipal on an FDA import alert?
- Yes. As of October 26, 2026, Cremeria Vero Interior Del Mercado Municipal is on the red list of FDA Import Alert 99-43, “Ready-to-eat foods: insanitary conditions”, for cheese/cheese products; FDA published the listing on August 27, 2025.
- Has FDA refused shipments from Cremeria Vero Interior Del Mercado Municipal?
- No FDA import refusals for Cremeria Vero Interior Del Mercado Municipal appear in FDA's refusal data since October 2016, as of October 26, 2026.
- What is Cremeria Vero Interior Del Mercado Municipal's FEI number?
- Cremeria Vero Interior Del Mercado Municipal's FDA Establishment Identifier (FEI) is 3003816149.
- Can shipments from Cremeria Vero Interior Del Mercado Municipal still enter the U.S.?
- Shipments of cheese/cheese products from Cremeria Vero Interior Del Mercado Municipal can be detained without physical examination under Import Alert 99-43; 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.