Reference Source

B.E.S. (BARCELONA EUROPE SUPPLY) · 99-39 · SPAIN

For B.E.S. (BARCELONA EUROPE SUPPLY) · 99-39 · SPAIN, import alert is 99-39; import alert name is Detention Without Physical Examination of Imported Food Products That Appear to Be Misbranded; country is SPAIN; product is Olives; product code is 21 G - - 09 Olives (Pit Fruit); date published is 07/24/2015; address is Enric Prat De La Riba, 12 Pol. Ind. Sala , Sant Boi De Llobregat , Barcelona, Cataluna SPAIN, verified against its source on 2026-09-16.

Firm
B.E.S. (BARCELONA EUROPE SUPPLY) verified
Import alert
99-39
Import alert name
Detention Without Physical Examination of Imported Food Products That Appear to Be Misbranded
Country
SPAIN verified
Address
Enric Prat De La Riba, 12 Pol. Ind. Sala , Sant Boi De Llobregat , Barcelona, Cataluna SPAIN verified
Date published
07/24/2015 verified
Product code
21 G - - 09 Olives (Pit Fruit) verified
Product
Olives verified
FDA notes
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be misbranded within the meaning of Section 403(f) of the Act in that all words; statements; and other information required by or under authority of the Act; on the label or labeling must appear there on in the English language as required by 21 CFR 101.15(c)(1). verified
Sourceaccessdata.fda.gov
Verified
Review by
DatasetFDA import alert red lists: firms subject to detention without physical examination

What the source says

B.E.S. (BARCELONA EUROPE SUPPLY) Date Published : 07/24/2015 Enric Prat De La Riba, 12 Pol. Ind. Sala , Sant Boi De Llobregat , Barcelona, Cataluna SPAIN 21 G - - 09 Olives (Pit Fruit) Date Published: 07/24/2015 Desc: Olives Notes: The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be misbranded within the meaning of Section 403(f) of the Act in that all words; statements; and other information required by or under authority of the Act; on the label or labeling must appear there on in the English language as required by 21 CFR 101.15(c)(1).

accessdata.fda.gov, retrieved 2026-09-15

Source

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