AB Nyakers Pepparkakor
FDA import alert and refusal historyBjurholm, SwedenFEI 3010358180
As of October 26, 2026, AB Nyakers Pepparkakor has no FDA import alert listing or import refusal in SupplierRadar's records; its most recent FDA inspection, on May 24, 2019, was classified VAI (Voluntary 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
- None found
- Last inspection
- Classified VAI (Voluntary Action Indicated)
Every FDA record for AB Nyakers Pepparkakor
2 records, newest first. Each line links to the FDA page it came from.
Questions about AB Nyakers Pepparkakor
- Is AB Nyakers Pepparkakor on an FDA import alert?
- No listing for AB Nyakers Pepparkakor appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Sweden page.
- Has FDA refused shipments from AB Nyakers Pepparkakor?
- No FDA import refusals for AB Nyakers Pepparkakor appear in FDA's refusal data since October 2016, as of October 26, 2026.
- When was AB Nyakers Pepparkakor last inspected by FDA?
- FDA's most recent inspection of AB Nyakers Pepparkakor with a final classification is dated May 24, 2019 and was classified VAI (Voluntary Action Indicated).
- What is AB Nyakers Pepparkakor's FEI number?
- AB Nyakers Pepparkakor's FDA Establishment Identifier (FEI) is 3010358180.
Buying from AB Nyakers Pepparkakor?
Watch it and get the FDA record the day it changes. Free for one supplier.
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.