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Sau To Brand Manufacturer

⚠️ High Risk

FEI: 3003998069 • Shenzhen City • CHINA

FEI

FEI Number

3003998069

📍

Location

Shenzhen City

🇨🇳

Country

CHINA
🏢

Address

Xin Tong Village, Da Shui Kengguan Lau, , Shenzhen City, , China

High Risk

FDA Import Risk Assessment

54.6
LowModerateHighCritical

This firm has a significant history of FDA import refusals with notable violations.

Statistics

16
Total Refusals
3
Unique Violations
5/12/2004
Latest Refusal
2/25/2004
Earliest Refusal

Score Breakdown

Violation Severity
77.4×40%
Refusal Volume
45.6×30%
Recency
0.0×20%
Frequency
100.0×10%
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

8315×

NO PROCESS

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the manufacturer's failure to file a scheduled process demonstrates that the product is not being manufactured under the mandatory provisions of 21 CFR Part 108 and therefore appears to have been manufactured, processed, or packed, under insanitary conditions whereby it may have been rendered injurious to health.

623×

NEEDS FCE

It appears the manufacturer is not registered as a low acid canned food or acidified food manufacturer pursuant to 21 CFR 108.25(c)(1) or 108.35(c)(1).

3201×

LACKS FIRM

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it appears to be misbranded within the meaning of Section 403(e)(1) of the FD&C Act in that the food is in package form and the label fails to bear the name and place of business of the manufacturer, packer, or distributor.

Refusal History

DateProductViolationsDivision
5/12/2004
29ACE99NONCARBONATED SOFT DRINK, N.E.C.
83NO PROCESS
San Francisco District Office (SAN-DO)
5/12/2004
29ACE99NONCARBONATED SOFT DRINK, N.E.C.
83NO PROCESS
San Francisco District Office (SAN-DO)
5/12/2004
29ACE99NONCARBONATED SOFT DRINK, N.E.C.
83NO PROCESS
San Francisco District Office (SAN-DO)
5/12/2004
29ACE99NONCARBONATED SOFT DRINK, N.E.C.
83NO PROCESS
San Francisco District Office (SAN-DO)
5/12/2004
29ACE99NONCARBONATED SOFT DRINK, N.E.C.
83NO PROCESS
San Francisco District Office (SAN-DO)
5/12/2004
29ACE99NONCARBONATED SOFT DRINK, N.E.C.
83NO PROCESS
San Francisco District Office (SAN-DO)
5/12/2004
29ACT99NONCARBONATED SOFT DRINK, N.E.C.
83NO PROCESS
Los Angeles District Office (LOS-DO)
5/12/2004
29ACT99NONCARBONATED SOFT DRINK, N.E.C.
83NO PROCESS
Los Angeles District Office (LOS-DO)
5/12/2004
29ACT99NONCARBONATED SOFT DRINK, N.E.C.
83NO PROCESS
Los Angeles District Office (LOS-DO)
5/12/2004
29ACT99NONCARBONATED SOFT DRINK, N.E.C.
83NO PROCESS
Los Angeles District Office (LOS-DO)
5/12/2004
29ACT99NONCARBONATED SOFT DRINK, N.E.C.
83NO PROCESS
Los Angeles District Office (LOS-DO)
5/12/2004
29ACT99NONCARBONATED SOFT DRINK, N.E.C.
83NO PROCESS
Los Angeles District Office (LOS-DO)
5/12/2004
29ACT99NONCARBONATED SOFT DRINK, N.E.C.
83NO PROCESS
Los Angeles District Office (LOS-DO)
5/12/2004
29ACT99NONCARBONATED SOFT DRINK, N.E.C.
62NEEDS FCE
Los Angeles District Office (LOS-DO)
2/25/2004
16ECT05SCALLOPS
320LACKS FIRM
62NEEDS FCE
83NO PROCESS
San Francisco District Office (SAN-DO)
2/25/2004
16ECT05SCALLOPS
62NEEDS FCE
83NO PROCESS
San Francisco District Office (SAN-DO)

Frequently Asked Questions

What is Sau To Brand Manufacturer's FDA import refusal history?

Sau To Brand Manufacturer (FEI: 3003998069) has 16 FDA import refusal record(s) in our database, spanning from 2/25/2004 to 5/12/2004.

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. Sau To Brand Manufacturer's FEI number is 3003998069.

What types of violations has Sau To Brand Manufacturer received?

Sau To Brand Manufacturer has been cited for 3 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 Sau To Brand Manufacturer come from?

All FDA import refusal data for Sau To Brand Manufacturer 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.