Arcor, SAIC

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

Refusal charges, in plain English

• LACKS FIRM1 refused line

  Manufacturer name and address missing

  The packaged product's label appeared not to show the name and place of business of the manufacturer, packer, or distributor.

• 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.

• LIST INGRE1 refused line

  Ingredients not listed

  The product is made from two or more ingredients and the label appeared not to list the common or usual name of each one (or, for a juice beverage, the percentage of juice).

• 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.

• UNSAFE COL1 refused line

  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.

• USUAL NAME1 refused line

  Common or usual name missing

  The label appeared not to show the common or usual name of the food.

Questions about Arcor, SAIC

Is Arcor, SAIC on an FDA import alert?

No listing for Arcor, SAIC appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Argentina page.

Has FDA refused shipments from Arcor, SAIC?

Yes. FDA refused 1 shipment line from Arcor, SAIC on June 2, 2017. The most recent, on June 2, 2017, was candy bar or pieces (not caramel or fondant), hard, without nuts and fruit (without chocolate), charged as UNSAFE COL (color additive unsafe under section 721).

Why did FDA refuse Arcor, SAIC's shipments?

The most frequent charges are LACKS FIRM (manufacturer name and address missing, 1 line) and LACKS N/C (net quantity statement missing, 1 line).

When was Arcor, SAIC last inspected by FDA?

FDA's most recent inspection of Arcor, SAIC with a final classification is dated December 15, 2015 and was classified NAI (No Action Indicated).

What is Arcor, SAIC's FEI number?

Arcor, SAIC's FDA Establishment Identifier (FEI) is 3004294587.