Parmalat Nicaragua, S.A.
FDA import alert and refusal historyManagua, NicaraguaFEI 1000585222
As of October 26, 2026, Parmalat Nicaragua, S.A. (Managua, Nicaragua) 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 28, 2025, 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 list
- Last import refusal
- None since October 2016
- Last warning letter
- None found
- Last inspection
- Classified NAI (No Action Indicated)
Every FDA record for Parmalat Nicaragua, S.A.
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
2013
- InspectionInspection classified NAI (No Action Indicated)Foodborne Biological HazardsSource
Questions about Parmalat Nicaragua, S.A.
- Is Parmalat Nicaragua, S.A. on an FDA import alert?
- Yes. As of October 26, 2026, Parmalat Nicaragua, S.A. 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 28, 2025.
- Has FDA refused shipments from Parmalat Nicaragua, S.A.?
- No FDA import refusals for Parmalat Nicaragua, S.A. appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was Parmalat Nicaragua, S.A. last inspected by FDA?
- FDA's most recent inspection of Parmalat Nicaragua, S.A. with a final classification is dated August 23, 2013 and was classified NAI (No Action Indicated).
- What is Parmalat Nicaragua, S.A.'s FEI number?
- Parmalat Nicaragua, S.A.'s FDA Establishment Identifier (FEI) is 1000585222.
- Can shipments from Parmalat Nicaragua, S.A. still enter the U.S.?
- Shipments of cheese/cheese products from Parmalat Nicaragua, S.A. 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.