Is Sheng Chang Pharmaceutical Co., Ltd. Zhongli Factory on an FDA import alert?

No listing for Sheng Chang Pharmaceutical Co., Ltd. Zhongli Factory appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Taiwan page.

Has FDA refused shipments from Sheng Chang Pharmaceutical Co., Ltd. Zhongli Factory?

Yes. FDA refused 6 shipment lines from Sheng Chang Pharmaceutical Co., Ltd. Zhongli Factory between October 20, 2016 and February 28, 2017. The most recent, on February 28, 2017, was ginseng (herbal & botanicals, not teas), charged as PESTICIDE (pesticide chemical residue).

Why did FDA refuse Sheng Chang Pharmaceutical Co., Ltd. Zhongli Factory's shipments?

The most frequent charges are POISONOUS (poisonous or deleterious substance, 2 lines) and UNAPPROVED (unapproved new drug, 2 lines).

When was Sheng Chang Pharmaceutical Co., Ltd. Zhongli Factory last inspected by FDA?

FDA's most recent inspection of Sheng Chang Pharmaceutical Co., Ltd. Zhongli Factory with a final classification is dated February 27, 2019 and was classified NAI (No Action Indicated).

Sheng Chang Pharmaceutical Co., Ltd. Zhongli Factory

FDA import alert and refusal historyTaoyuan City, TaiwanFEI 3011382182

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As of October 26, 2026, Sheng Chang Pharmaceutical Co., Ltd. Zhongli Factory is not on any FDA import alert in SupplierRadar's records; FDA refused 6 of its shipment lines between October 20, 2016 and February 28, 2017, most often for poisonous or deleterious substance (POISONOUS).

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

Current status

Import alerts: Not listed
Last import refusal: Feb 28, 2017Ginseng (herbal & botanicals, not teas) · PESTICIDE
Last warning letter: None found
Last inspection: Feb 27, 2019Classified NAI (No Action Indicated)

Every FDA record for Sheng Chang Pharmaceutical Co., Ltd. Zhongli Factory

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

2019

Feb 27, 2019Inspection
Inspection classified NAI (No Action Indicated)Food Composition, Standards, Labeling and Econ; Foodborne Biological Hazards
Source

2017

Feb 28, 2017Import refusal
Refused, Ginseng (herbal & botanicals, not teas)PESTICIDEEntry ES3-2500138-7
Source

2016

Oct 20, 2016Import refusal
Refused, Herbals & botanicals (not teas), n.e.c.POISONOUSEntry ES3-2101408-7
Source
Oct 20, 2016Import refusal
Refused, Stephania (fangji), (herbal & botanicals, not teas)UNAPPROVEDEntry ES3-2100296-7
Source
Oct 20, 2016Import refusal
Refused, Herbals & botanicals (not teas), n.e.c.EPHEDALKEntry ES3-2101408-7
Source
Oct 20, 2016Import refusal
Refused, Herbals & botanicals (not teas), n.e.c.UNAPPROVEDEntry ES3-2100296-7
Source
Oct 20, 2016Import refusal
Refused, Herbals & botanicals (not teas), n.e.c.POISONOUSEntry ES3-2101408-7
Source

Refusal charges, in plain English

POISONOUS2 refused lines
Poisonous or deleterious substance
The product appeared to bear or contain a poisonous or deleterious substance which may render it injurious to health.
UNAPPROVED2 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.
EPHEDALK1 refused line
EPHEDALK
PESTICIDE1 refused line
Pesticide chemical residue
The product appeared to contain a pesticide chemical residue that makes it adulterated under section 402(a)(2)(B) of the FD&C Act, for example a residue above the U.S. tolerance or one with no U.S. tolerance for that food.

Questions about Sheng Chang Pharmaceutical Co., Ltd. Zhongli Factory

Is Sheng Chang Pharmaceutical Co., Ltd. Zhongli Factory on an FDA import alert?: No listing for Sheng Chang Pharmaceutical Co., Ltd. Zhongli Factory appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Taiwan page.
Has FDA refused shipments from Sheng Chang Pharmaceutical Co., Ltd. Zhongli Factory?: Yes. FDA refused 6 shipment lines from Sheng Chang Pharmaceutical Co., Ltd. Zhongli Factory between October 20, 2016 and February 28, 2017. The most recent, on February 28, 2017, was ginseng (herbal & botanicals, not teas), charged as PESTICIDE (pesticide chemical residue).
Why did FDA refuse Sheng Chang Pharmaceutical Co., Ltd. Zhongli Factory's shipments?: The most frequent charges are POISONOUS (poisonous or deleterious substance, 2 lines) and UNAPPROVED (unapproved new drug, 2 lines).
When was Sheng Chang Pharmaceutical Co., Ltd. Zhongli Factory last inspected by FDA?: FDA's most recent inspection of Sheng Chang Pharmaceutical Co., Ltd. Zhongli Factory with a final classification is dated February 27, 2019 and was classified NAI (No Action Indicated).
What is Sheng Chang Pharmaceutical Co., Ltd. Zhongli Factory's FEI number?: Sheng Chang Pharmaceutical Co., Ltd. Zhongli Factory's FDA Establishment Identifier (FEI) is 3011382182.

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