Sunsho Pharmaceutical Co. (Fujine Factory)

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

Refusal charges, in plain English

• UNAPPROVED1 refused line

  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.

Questions about Sunsho Pharmaceutical Co. (Fujine Factory)

Is Sunsho Pharmaceutical Co. (Fujine Factory) on an FDA import alert?

No listing for Sunsho Pharmaceutical Co. (Fujine Factory) appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Japan page.

Has FDA refused shipments from Sunsho Pharmaceutical Co. (Fujine Factory)?

Yes. FDA refused 1 shipment line from Sunsho Pharmaceutical Co. (Fujine Factory) on February 23, 2026. The most recent, on February 23, 2026, was foods (including water) with excessive nutritional claims, charged as UNAPPROVED (unapproved new drug).

Why did FDA refuse Sunsho Pharmaceutical Co. (Fujine Factory)'s shipments?

The most frequent charge is UNAPPROVED (unapproved new drug, 1 line).

When was Sunsho Pharmaceutical Co. (Fujine Factory) last inspected by FDA?

FDA's most recent inspection of Sunsho Pharmaceutical Co. (Fujine Factory) with a final classification is dated April 23, 2026 and was classified NAI (No Action Indicated).

What is Sunsho Pharmaceutical Co. (Fujine Factory)'s FEI number?

Sunsho Pharmaceutical Co. (Fujine Factory)'s FDA Establishment Identifier (FEI) is 3014135556.