FILARETOS BROS CO. · 16-120 · GREECE
For FILARETOS BROS CO. · 16-120 · GREECE, import alert is 16-120; import alert name is "Detention Without Physical Examination of ***Fish and Fishery*** Products from Foreign Processors (Mfrs.) Not in Compliance with Seafood HACCP ***Regulation***"; country is GREECE; product is Refrigerated RTE marinated anchovies in oil - not thermally processed | RTE cold-smoked herring in vacuum packaging; product code is 16 A - - 01 Anchovy | 16 S V - 21 Herring, Cold Smoked, Fish, Vacuum or Modified Atmosphere Packaging; date published is 06/22/2026; address is Asminio , Istiaia, Sterea Ellada GREECE, verified against its source on 2026-09-16.
- Firm
- FILARETOS BROS CO. verified
- Import alert
- 16-120
- Import alert name
- "Detention Without Physical Examination of ***Fish and Fishery*** Products from Foreign Processors (Mfrs.) Not in Compliance with Seafood HACCP ***Regulation***"
- Country
- GREECE verified
- Address
- Asminio , Istiaia, Sterea Ellada GREECE verified
- Date published
- 06/22/2026 verified
- Product code
- 16 A - - 01 Anchovy | 16 S V - 21 Herring, Cold Smoked, Fish, Vacuum or Modified Atmosphere Packaging each item verified
- Product
- Refrigerated RTE marinated anchovies in oil - not thermally processed | RTE cold-smoked herring in vacuum packaging each item verified
- FDA notes
- FDA inspection of this food manufacturing facility found serious deviations of the seafood HACCP regulations (21 CFR Part 123). Based on FDA’s inspectional findings and review of the firm’s response, the FDA determined that the firm’s Refrigerated RTE marinated anchovies in oil (not thermally processed) and RTE cold-smoked herring in vacuum packaging processed in the facility appear to be adulterated within the meaning of section 402(a)(4) of the Federal Food, Drug, and Cosmetic Act. Identified violations include: 21 CFR 123.6(c)(3), inadequate critical limit and 21 CFR 123.6(c)(2), failure to identify CCP(s). | FDA inspection of this food manufacturing facility found serious deviations of the seafood HACCP regulations (21 CFR Part 123). Based on FDA’s inspectional findings and review of the firm’s response, the FDA determined that the firm’s Refrigerated RTE marinated anchovies in oil (not thermally processed) and RTE cold-smoked herring in vacuum packaging processed in the facility appear to be adulterated within the meaning of section 402(a)(4) of the Federal Food, Drug, and Cosmetic Act. Identified violations include: 21 CFR 123.6(c)(3), inadequate critical limit and 21 CFR 123.6(c)(2), failure to identify CCP(s). each item verified
What the source says
FILARETOS BROS CO. Date Published : 06/22/2026 Asminio , Istiaia, Sterea Ellada GREECE 16 A - - 01 Anchovy Date Published: 06/22/2026 Desc: Refrigerated RTE marinated anchovies in oil - not thermally processed Notes: FDA inspection of this food manufacturing facility found serious deviations of the seafood HACCP regulations (21 CFR Part 123). Based on FDA’s inspectional findings and review of the firm’s response, the FDA determined that the firm’s Refrigerated RTE marinated anchovies in oil (not thermally processed) and RTE cold-smoked herring in vacuum packaging processed in the facility appear to be adulterated within the meaning of section 402(a)(4) of the Federal Food, Drug, and Cosmetic Act. Identified violations include: 21 CFR 123.6(c)(3), inadequate critical limit and 21 CFR 123.6(c)(2), failure to identify CCP(s). 16 S V - 21 Herring, Cold Smoked, Fish, Vacuum or Modified Atmosphere Packaging Date Published: 06/22/2026 Desc: RTE cold-smoked herring in vacuum packaging Notes: FDA inspection of this food manufacturing facility found serious deviations of the seafood HACCP regulations (21 CFR Part 123). Based on FDA’s inspectional findings and review of the firm’s response, the FDA determined that the firm’s Refrigerated RTE marinated anchovies in oil (not thermally processed) and RTE cold-smoked herring in vacuum packaging processed in the facility appear to be adulterated within the meaning of section 402(a)(4) of the Federal Food, Drug, and Cosmetic Act. Identified violations include: 21 CFR 123.6(c)(3), inadequate critical limit and 21 CFR 123.6(c)(2), failure to identify CCP(s).
— accessdata.fda.gov, retrieved 2026-09-01
Source
- accessdata.fda.govhttps://www.accessdata.fda.gov/cms_ia/importalert_25.html
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