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AB Boviks Konservfabriker

FDA import alert and refusal historyLysekil, SwedenFEI 11106

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Example subjectAB Boviks Konservfabrike added to Import Alert 16-129 (red list)

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As of October 26, 2026, AB Boviks Konservfabriker (Lysekil, Sweden) is on the red list of FDA Import Alert 99-37 (Low-acid canned/acidified foods without scheduled process) for fish dumpling in boullion, published by FDA on June 3, 2014, and has no FDA import refusals recorded since October 2016.

Data from FDA public records, last checked . Request a correction

Current status

Last import refusal
None since October 2016
Last warning letter
None found
Last inspection
None on record

Every FDA record for AB Boviks Konservfabriker

1 record, newest first. Each line links to the FDA page it came from.

2014

  1. Import alert listing
    Listed on Import Alert 99-37red listFish dumpling in boullion
    Source

Questions about AB Boviks Konservfabriker

Is AB Boviks Konservfabriker on an FDA import alert?
Yes. As of October 26, 2026, AB Boviks Konservfabriker is on the red list of FDA Import Alert 99-37, “Low-acid canned/acidified foods without scheduled process”, for fish dumpling in boullion; FDA published the listing on June 3, 2014.
Has FDA refused shipments from AB Boviks Konservfabriker?
No FDA import refusals for AB Boviks Konservfabriker appear in FDA's refusal data since October 2016, as of October 26, 2026.
What is AB Boviks Konservfabriker's FEI number?
AB Boviks Konservfabriker's FDA Establishment Identifier (FEI) is 11106.
Can shipments from AB Boviks Konservfabriker still enter the U.S.?
Shipments of fish dumpling in boullion from AB Boviks Konservfabriker can be detained without physical examination under Import Alert 99-37; 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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Example subjectAB Boviks Konservfabrike added to Import Alert 16-129 (red list)

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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.