Bridor SAS

13 records, newest first. Each line links to the FDA page it came from.

Refusal charges, in plain English

• UNSAFE COL11 refused lines

  Color additive unsafe under section 721

  The product appeared to be, or to contain, a color additive that is unsafe within the meaning of section 721(a) of the FD&C Act, the section that governs which color additives may be used and how.

• FALSE1 refused line

  False or misleading labeling

  The labeling appeared to be false or misleading in some particular.

• LACKS N/C1 refused line

  Net quantity statement missing

  The packaged food appeared not to carry an accurate statement of the quantity of contents, such as net weight, measure, or count, on its label.

• NUTRIT LBL1 refused line

  Nutrition information missing from label

  The label or labeling appeared not to carry the nutrition information that U.S. law requires for the food.

Questions about Bridor SAS

Is Bridor SAS on an FDA import alert?

No listing for Bridor SAS appears in the FDA import alerts SupplierRadar checked on October 25, 2026. Country-wide alerts may still apply to its products; see the France page.

Has FDA refused shipments from Bridor SAS?

Yes. FDA refused 11 shipment lines from Bridor SAS between November 20, 2017 and May 21, 2020. The most recent, on May 21, 2020, was macaroon,filled or iced cookies, biscuits and wafers, charged as UNSAFE COL (color additive unsafe under section 721).

Why did FDA refuse Bridor SAS's shipments?

The most frequent charges are UNSAFE COL (color additive unsafe under section 721, 11 lines) and FALSE (false or misleading labeling, 1 line).

When was Bridor SAS last inspected by FDA?

FDA's most recent inspection of Bridor SAS with a final classification is dated September 7, 2023 and was classified NAI (No Action Indicated).

What is Bridor SAS's FEI number?

Bridor SAS's FDA Establishment Identifier (FEI) is 3005153639.