CV Melda Family

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

Refusal charges, in plain English

• UNSFDIETSP6 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.

• UNAPPROVED3 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.

• UNSAFE ADD3 refused lines

  Food additive unsafe under section 409

  The product appeared to contain a food additive that is unsafe within the meaning of section 409 of the FD&C Act, the section that governs which food additives may be used and under what conditions.

• DIRSEXMPT1 refused line

  DIRSEXMPT

• NDIDIETSP1 refused line

  NDIDIETSP

Questions about CV Melda Family

Is CV Melda Family on an FDA import alert?

No listing for CV Melda Family 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 CV Melda Family?

Yes. FDA refused 10 shipment lines from CV Melda Family between February 16, 2021 and March 22, 2022. The most recent, on March 22, 2022, was kratom (herbal and botanicals, not teas ii), charged as UNSAFE ADD (food additive unsafe under section 409).

Why did FDA refuse CV Melda Family's shipments?

The most frequent charges are UNSFDIETSP (dietary ingredient without safety assurance, 6 lines) and UNAPPROVED (unapproved new drug, 3 lines).

What is CV Melda Family's FEI number?

CV Melda Family's FDA Establishment Identifier (FEI) is 3018549424.