ImportRefusal LogoImportRefusal

Shandong Bouliga Biotechnology Co.,Ltd

⚠️ Moderate Risk

FEI: 3011894901 • Jining, Shandong • CHINA

FEI

FEI Number

3011894901

📍

Location

Jining, Shandong

🇨🇳

Country

CHINA
🏢

Address

Wucun, Qufu, Jining, Shandong, China

Moderate Risk

FDA Import Risk Assessment

31.3
LowModerateHighCritical

This firm has a moderate history of FDA import refusals. Some attention may be warranted.

Statistics

2
Total Refusals
7
Unique Violations
12/13/2019
Latest Refusal
5/7/2019
Earliest Refusal

Score Breakdown

Violation Severity
60.0×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
20.0×10%
How is this score calculated?

Proprietary Algorithm

  • 40% Violation Severity — AI-assessed (1-10)
  • 30% Refusal Volume — Logarithmic scale
  • 20% Recency — Decays over 5 years
  • 10% Frequency — Refusals per year

© ImportRefusal.com Original Analysis

Violation Summary

1181×

NOT LISTED

It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).

161×

DIRECTIONS

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose label appears to not bear adequate directions for use.

2371×

NO PMA

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the device appears to be a Class III device and does not appear to have in effect an approved application for premarket approval pursuant to Section 515 of the Act, or an exemption pursuant to Section 520(g)(1).

24801×

RXPERSONAL

The article appears to be a device which requires a prescription from your doctor.

32801×

FRNMFGREG

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.

3331×

LACKS FIRM

The article is in package form and appears to not bear a label containing the name and place of business of the manufacturer, packer, or distributor.

721×

NEW VET DR

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the Federal Food, Drug, and Cosmetic Act in that it appears to be a new animal drug that is unsafe within the meaning of Section 512(a) of the Federal Food, Drug, and Cosmetic Act as it is not the subject of an approved new animal drug application, conditionally approved new animal drug application, or index listing, and no investigational new animal drug exemption applies.

Refusal History

DateProductViolationsDivision
12/13/2019
66MRY28DROPERIDOL (TRANQUILIZER)
72NEW VET DR
Division of Southeast Imports (DSEI)
5/7/2019
79LMHIMPLANT, DERMAL, COLLAGEN FOR AESTHETIC USE
118NOT LISTED
16DIRECTIONS
237NO PMA
2480RXPERSONAL
3280FRNMFGREG
333LACKS FIRM
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is Shandong Bouliga Biotechnology Co.,Ltd's FDA import refusal history?

Shandong Bouliga Biotechnology Co.,Ltd (FEI: 3011894901) has 2 FDA import refusal record(s) in our database, spanning from 5/7/2019 to 12/13/2019.

What is an FEI number?

FEI stands for Firm Establishment Identifier. It's a unique number assigned by the FDA to identify establishments that manufacture, process, pack, or hold food, drugs, medical devices, or other FDA-regulated products. Shandong Bouliga Biotechnology Co.,Ltd's FEI number is 3011894901.

What types of violations has Shandong Bouliga Biotechnology Co.,Ltd received?

Shandong Bouliga Biotechnology Co.,Ltd has been cited for 7 different violation type(s). Common FDA violations include adulteration (unsafe or unsanitary products), misbranding (incorrect or misleading labels), and regulatory non-compliance.

Where does this information about Shandong Bouliga Biotechnology Co.,Ltd come from?

All FDA import refusal data for Shandong Bouliga Biotechnology Co.,Ltd is sourced from the official FDA Data Dashboard (datadashboard.fda.gov), a public government database maintained by the U.S. Food and Drug Administration.

Data sourced from the FDA Data Dashboard, a public database maintained by the U.S. Food and Drug Administration.