Adi Dharma Putra

6 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.

• UNAPPROVED2 refused lines

  Unapproved new drug

  The product appeared to be a new drug within the meaning of section 201(p) of the FD&C Act without an approved New Drug Application. FDA can apply this charge to a food or supplement whose labeling presents it for drug uses.

• DIRECTIONS1 refused line

  DIRECTIONS

• DIRSEXMPT1 refused line

  DIRSEXMPT

• 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.

Questions about Adi Dharma Putra

Is Adi Dharma Putra on an FDA import alert?

No listing for Adi Dharma Putra 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 Adi Dharma Putra?

Yes. FDA refused 6 shipment lines from Adi Dharma Putra between December 27, 2016 and June 3, 2020. The most recent, on June 3, 2020, was kratom (herbal and botanicals, not teas ii), charged as DIRSEXMPT (dirsexmpt).

Why did FDA refuse Adi Dharma Putra's shipments?

The most frequent charges are UNSFDIETSP (dietary ingredient without safety assurance, 4 lines) and UNAPPROVED (unapproved new drug, 2 lines).

What is Adi Dharma Putra's FEI number?

Adi Dharma Putra's FDA Establishment Identifier (FEI) is 3011772014.