Bioherbs C.I. E.U

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

Refusal charges, in plain English

• PESTICIDE2 refused lines

  Pesticide chemical residue

  The product appeared to contain a pesticide chemical residue that makes it adulterated under section 402(a)(2)(B) of the FD&C Act, for example a residue above the U.S. tolerance or one with no U.S. tolerance for that food.

• 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.

Questions about Bioherbs C.I. E.U

Is Bioherbs C.I. E.U on an FDA import alert?

Yes. As of October 25, 2026, Bioherbs C.I. E.U is on the red list of FDA Import Alert 99-05, “Raw agricultural products: pesticides”, for thyme; FDA published the listing on January 18, 2023.

Has FDA refused shipments from Bioherbs C.I. E.U?

Yes. FDA refused 2 shipment lines from Bioherbs C.I. E.U on January 24, 2023. The most recent, on January 24, 2023, was thyme, whole (spice), charged as PESTICIDE (pesticide chemical residue).

Why did FDA refuse Bioherbs C.I. E.U's shipments?

The most frequent charges are PESTICIDE (pesticide chemical residue, 2 lines) and LACKS FIRM (manufacturer name and address missing, 1 line).

When was Bioherbs C.I. E.U last inspected by FDA?

FDA's most recent inspection of Bioherbs C.I. E.U with a final classification is dated December 17, 2010 and was classified VAI (Voluntary Action Indicated).

What is Bioherbs C.I. E.U's FEI number?

Bioherbs C.I. E.U's FDA Establishment Identifier (FEI) is 3004687274.

Can shipments from Bioherbs C.I. E.U still enter the U.S.?

Shipments of thyme from Bioherbs C.I. E.U can be detained without physical examination under Import Alert 99-05; 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).