Akita Herbal Products

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

Refusal charges, in plain English

• UNSFDIETSP2 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.

• PLANT PART1 refused line

  PLANT PART

Questions about Akita Herbal Products

Is Akita Herbal Products on an FDA import alert?

Yes. As of October 26, 2026, Akita Herbal Products is on the red list of FDA Import Alert 54-15, “Supplements and ingredients containing kratom”, for serenoa 330-350mg capsules (food supplements); FDA published the listing on December 19, 2016.

Has FDA refused shipments from Akita Herbal Products?

Yes. FDA refused 2 shipment lines from Akita Herbal Products between October 27, 2016 and February 23, 2018. The most recent, on February 23, 2018, was herbals & botanicals (not teas), n.e.c., charged as UNSFDIETSP (dietary ingredient without safety assurance).

Why did FDA refuse Akita Herbal Products's shipments?

The most frequent charges are UNSFDIETSP (dietary ingredient without safety assurance, 2 lines) and PLANT PART (plant part, 1 line).

What is Akita Herbal Products's FEI number?

Akita Herbal Products's FDA Establishment Identifier (FEI) is 3010886839.

Can shipments from Akita Herbal Products still enter the U.S.?

Shipments of serenoa 330-350mg capsules (food supplements) from Akita Herbal Products can be detained without physical examination under Import Alert 54-15; 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).