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Arsy CV

FDA import alert and refusal historyBekasi, IndonesiaFEI 3011765542

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Example subjectArsy C added to Import Alert 16-129 (red list)

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As of October 26, 2026, Arsy CV is not on any FDA import alert in SupplierRadar's records; FDA refused 8 of its shipment lines between October 4, 2016 and July 13, 2020, most often for dietary ingredient without safety assurance (UNSFDIETSP).

Data from FDA public records, last checked . Request a correction

Current status

Import alerts
Not listed
Last import refusal
Kratom (herbal and botanicals, not teas ii) · UNSFDIETSP
Last warning letter
None found
Last inspection
None on record

Every FDA record for Arsy CV

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

2020

  1. Import refusal
    Refused, Kratom (herbal and botanicals, not teas ii)UNSFDIETSPEntry AEK-2294121-2
    Source

2017

  1. Import refusal
    Refused, Kratom (herbal and botanicals, not teas ii)UNSFDIETSPLIST INGRELACKS FIRMLABELINGEntry 799-9527214-8
    Source
  2. Import refusal
    Refused, Kratom (herbal and botanicals, not teas ii)UNSFDIETSPLIST INGRELACKS FIRMSTD NAMELABELINGEntry 799-9523605-1
    Source
  3. Import refusal
    Refused, Kratom (herbal and botanicals, not teas ii)LIST INGREUNSFDIETLBLACKS FIRMSTD NAMELABELINGEntry 799-9512525-4
    Source
  4. Import refusal
    Refused, Kratom (herbal and botanical teas ii, continued)UNSAFE ADDEntry 799-9512658-3
    Source
  5. Import refusal
    Refused, Kratom (herbal and botanicals, not teas ii)UNSFDIETSPLIST INGRELACKS FIRMSTD NAMELABELINGEntry 799-9518923-5
    Source
  6. Import refusal
    Refused, Kratom (herbal and botanicals, not teas ii)UNSFDIETSPEntry AEK-2252062-8
    Source

2016

  1. Import refusal
    Refused, Kratom (herbal and botanicals, not teas ii)UNSFDIETSPEntry AEK-2259713-9
    Source

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.

  • LABELING4 refused lines

    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.

  • LACKS FIRM4 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.

  • LIST INGRE4 refused lines

    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).

  • STD NAME3 refused lines

    STD NAME

  • UNSAFE ADD1 refused line

    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.

  • UNSFDIETLB1 refused line

    UNSFDIETLB

Questions about Arsy CV

Is Arsy CV on an FDA import alert?
No listing for Arsy CV 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 Arsy CV?
Yes. FDA refused 8 shipment lines from Arsy CV between October 4, 2016 and July 13, 2020. The most recent, on July 13, 2020, was kratom (herbal and botanicals, not teas ii), charged as UNSFDIETSP (dietary ingredient without safety assurance).
Why did FDA refuse Arsy CV's shipments?
The most frequent charges are UNSFDIETSP (dietary ingredient without safety assurance, 6 lines) and LABELING (fair packaging and labeling act, 4 lines).
What is Arsy CV's FEI number?
Arsy CV's FDA Establishment Identifier (FEI) is 3011765542.

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SupplierRadar is not affiliated with the U.S. Food and Drug Administration. Data comes from public FDA records and may contain errors. This is not legal advice; importers remain responsible for their supplier evaluations.