Pharmtech Korea

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

Refusal charges, in plain English

• 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.

Questions about Pharmtech Korea

Is Pharmtech Korea on an FDA import alert?

Yes. As of October 26, 2026, Pharmtech Korea is on the red list of FDA Import Alert 99-39, “Imported foods that appear to be misbranded”, for imperial be collagen; FDA published the listing on March 30, 2020.

Has FDA refused shipments from Pharmtech Korea?

Yes. FDA refused 1 shipment line from Pharmtech Korea on December 1, 2025. The most recent, on December 1, 2025, was animal by-products and extracts, n.e.c., charged as UNSAFE ADD (food additive unsafe under section 409).

Why did FDA refuse Pharmtech Korea's shipments?

The most frequent charge is UNSAFE ADD (food additive unsafe under section 409, 1 line).

What is Pharmtech Korea's FEI number?

Pharmtech Korea's FDA Establishment Identifier (FEI) is 3010523680.

Can shipments from Pharmtech Korea still enter the U.S.?

Shipments of imperial be collagen from Pharmtech Korea can be detained without physical examination under Import Alert 99-39; 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).