Myllan-ORA ehf
FDA import alert and refusal historyKopavogur, IcelandFEI 3001017171
As of October 26, 2026, Myllan-ORA ehf has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on May 25, 2022, was classified OAI (Official Action Indicated).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- None since October 2016
- Last warning letter
- Seafood HACCP/CGMP for Foods/Adulterated/Insanitary Conditions
- Last inspection
- Classified OAI (Official Action Indicated)
Every FDA record for Myllan-ORA ehf
4 records, newest first. Each line links to the FDA page it came from.
Questions about Myllan-ORA ehf
- Is Myllan-ORA ehf on an FDA import alert?
- No listing for Myllan-ORA ehf appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Iceland page.
- Has FDA refused shipments from Myllan-ORA ehf?
- No FDA import refusals for Myllan-ORA ehf appear in FDA's refusal data since October 2016, as of October 26, 2026.
- Has Myllan-ORA ehf received an FDA warning letter?
- Yes. FDA issued a warning letter to Myllan-ORA ehf on August 30, 2022 (Seafood HACCP/CGMP for Foods/Adulterated/Insanitary Conditions).
- When was Myllan-ORA ehf last inspected by FDA?
- FDA's most recent inspection of Myllan-ORA ehf with a final classification is dated May 25, 2022 and was classified OAI (Official Action Indicated).
- What is Myllan-ORA ehf's FEI number?
- Myllan-ORA ehf's FDA Establishment Identifier (FEI) is 3001017171.
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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.