Is Kolmar Bnh Co.,Ltd.(Sbt) on an FDA import alert?

No listing for Kolmar Bnh Co.,Ltd.(Sbt) appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the South Korea page.

Has FDA refused shipments from Kolmar Bnh Co.,Ltd.(Sbt)?

Yes. FDA refused 6 shipment lines from Kolmar Bnh Co.,Ltd.(Sbt) between August 8, 2018 and March 2, 2020. The most recent, on March 2, 2020, was vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c., charged as NCONTACT (no u.s. adverse event contact on supplement label).

Why did FDA refuse Kolmar Bnh Co.,Ltd.(Sbt)'s shipments?

The most frequent charges are UNAPPROVED (unapproved new drug, 6 lines) and HEALTH C (unauthorized nutrient content or health claim, 2 lines).

When was Kolmar Bnh Co.,Ltd.(Sbt) last inspected by FDA?

FDA's most recent inspection of Kolmar Bnh Co.,Ltd.(Sbt) with a final classification is dated July 22, 2024 and was classified NAI (No Action Indicated).

What is Kolmar Bnh Co.,Ltd.(Sbt)'s FEI number?

Kolmar Bnh Co.,Ltd.(Sbt)'s FDA Establishment Identifier (FEI) is 3010128151.

Kolmar Bnh Co.,Ltd.(Sbt)

FDA import alert and refusal historySejong, South KoreaFEI 3010128151

Recorded by FDA as KOLMAR BNH CO.,LTD.(SBT)

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As of October 26, 2026, Kolmar Bnh Co.,Ltd.(Sbt) is not on any FDA import alert in SupplierRadar's records; FDA refused 6 of its shipment lines between August 8, 2018 and March 2, 2020, most often for unapproved new drug (UNAPPROVED).

Data from FDA public records, last checked October 26, 2026. Request a correction

Current status

Import alerts: Not listed
Last import refusal: Mar 2, 2020Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c. · NCONTACT
Last warning letter: None found
Last inspection: Jul 22, 2024Classified NAI (No Action Indicated)

Every FDA record for Kolmar Bnh Co.,Ltd.(Sbt)

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

2024

Jul 22, 2024Inspection
Inspection classified NAI (No Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological Hazards
Source

2020

Mar 2, 2020Import refusal
Refused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.NCONTACT NUTRIT LBL HEALTH C UNAPPROVEDEntry SCS-8853533-2
Source
Mar 2, 2020Import refusal
Refused, Vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c.NCONTACT NUTRIT LBL HEALTH C UNAPPROVEDEntry SCS-8852747-9
Source

2019

Jun 20, 2019Import refusal
Refused, Angelica (herbal & botanicals, not teas)PLANT PART UNAPPROVEDEntry MR5-2048809-6
Source
May 28, 2019Import refusal
Refused, Angelica (herbal & botanicals, not teas)UNAPPROVEDEntry MR5-2048493-9
Source
Apr 10, 2019Inspection
Inspection classified VAI (Voluntary Action Indicated)Food Composition, Standards, Labeling and Econ
Source

2018

Aug 31, 2018Import refusal
Refused, Angelica (herbal & botanicals, not teas)UNAPPROVEDEntry AEK-5088231-2
Source
Aug 8, 2018Import refusal
Refused, Angelica (herbal & botanicals, not teas)DIRECTIONS UNAPPROVEDEntry MR5-2042893-6
Source

Refusal charges, in plain English

UNAPPROVED6 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.
HEALTH C2 refused lines
Unauthorized nutrient content or health claim
The label or labeling appeared to carry a nutrient content claim or health claim that is not authorized.
NCONTACT2 refused lines
No U.S. adverse event contact on supplement label
The dietary supplement label appeared not to show a U.S. address or phone number through which a serious adverse event can be reported.
NUTRIT LBL2 refused lines
Nutrition information missing from label
The label or labeling appeared not to carry the nutrition information that U.S. law requires for the food.
DIRECTIONS1 refused line
DIRECTIONS
PLANT PART1 refused line
PLANT PART

Questions about Kolmar Bnh Co.,Ltd.(Sbt)

Is Kolmar Bnh Co.,Ltd.(Sbt) on an FDA import alert?: No listing for Kolmar Bnh Co.,Ltd.(Sbt) appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the South Korea page.
Has FDA refused shipments from Kolmar Bnh Co.,Ltd.(Sbt)?: Yes. FDA refused 6 shipment lines from Kolmar Bnh Co.,Ltd.(Sbt) between August 8, 2018 and March 2, 2020. The most recent, on March 2, 2020, was vitamin, mineral, proteins and unconventional dietary specialities for humans and animals, n.e.c., charged as NCONTACT (no u.s. adverse event contact on supplement label).
Why did FDA refuse Kolmar Bnh Co.,Ltd.(Sbt)'s shipments?: The most frequent charges are UNAPPROVED (unapproved new drug, 6 lines) and HEALTH C (unauthorized nutrient content or health claim, 2 lines).
When was Kolmar Bnh Co.,Ltd.(Sbt) last inspected by FDA?: FDA's most recent inspection of Kolmar Bnh Co.,Ltd.(Sbt) with a final classification is dated July 22, 2024 and was classified NAI (No Action Indicated).
What is Kolmar Bnh Co.,Ltd.(Sbt)'s FEI number?: Kolmar Bnh Co.,Ltd.(Sbt)'s FDA Establishment Identifier (FEI) is 3010128151.

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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.