Deki Oktavianto

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

Refusal charges, in plain English

• UNSFDIETSP4 refused lines

  Dietary ingredient without safety assurance

  The product appeared to be a dietary supplement or dietary ingredient for which there is inadequate information to provide reasonable assurance that it does not present a significant or unreasonable risk of illness or injury.

• LACKS FIRM2 refused lines

  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.

• FALSE1 refused line

  False or misleading labeling

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

• INCONSPICU1 refused line

  Required information not conspicuous

  Information required on the label appeared not to be placed prominently or conspicuously enough to be read and understood by an ordinary consumer.

• LABELING1 refused line

  Fair Packaging and Labeling Act

  The package appeared not to meet the Fair Packaging and Labeling Act because of the placement, form, or contents of a required label statement.

• 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).

Questions about Deki Oktavianto

Is Deki Oktavianto on an FDA import alert?

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

Has FDA refused shipments from Deki Oktavianto?

Yes. FDA refused 5 shipment lines from Deki Oktavianto between November 10, 2020 and June 22, 2021. The most recent, on June 22, 2021, was kratom (herbal and botanicals, not teas ii), charged as UNSFDIETSP (dietary ingredient without safety assurance).

Why did FDA refuse Deki Oktavianto's shipments?

The most frequent charges are UNSFDIETSP (dietary ingredient without safety assurance, 4 lines) and LACKS FIRM (manufacturer name and address missing, 2 lines).

What is Deki Oktavianto's FEI number?

Deki Oktavianto's FDA Establishment Identifier (FEI) is 3017000002.