AB "Zemaitijos pienas"
FDA import alert and refusal historyTelsiai, LithuaniaFEI 3004326531
As of October 26, 2026, AB "Zemaitijos pienas" (Telsiai, Lithuania) is on the red list of FDA Import Alert 99-45 (Foods that are or contain an unsafe food additive) for palanga cheese, published by FDA on March 28, 2022, 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 99-45 · 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 AB "Zemaitijos pienas"
2 records, newest first. Each line links to the FDA page it came from.
2022
- InspectionInspection classified NAI (No Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological HazardsSource
- Import alert listingListed on Import Alert 99-45red listPalanga CheeseSource
Questions about AB "Zemaitijos pienas"
- Is AB "Zemaitijos pienas" on an FDA import alert?
- Yes. As of October 26, 2026, AB "Zemaitijos pienas" is on the red list of FDA Import Alert 99-45, “Foods that are or contain an unsafe food additive”, for palanga cheese; FDA published the listing on March 28, 2022.
- Has FDA refused shipments from AB "Zemaitijos pienas"?
- No FDA import refusals for AB "Zemaitijos pienas" appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was AB "Zemaitijos pienas" last inspected by FDA?
- FDA's most recent inspection of AB "Zemaitijos pienas" with a final classification is dated July 1, 2022 and was classified NAI (No Action Indicated).
- What is AB "Zemaitijos pienas"'s FEI number?
- AB "Zemaitijos pienas"'s FDA Establishment Identifier (FEI) is 3004326531.
- Can shipments from AB "Zemaitijos pienas" still enter the U.S.?
- Shipments of palanga cheese from AB "Zemaitijos pienas" can be detained without physical examination under Import Alert 99-45; 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.