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PT ASI Pudjiastuti

⚠️ High Risk

FEI: 3004677781 • Pangandaran, None of the above • INDONESIA

FEI

FEI Number

3004677781

📍

Location

Pangandaran, None of the above

🇮🇩

Country

INDONESIA
🏢

Address

Jalan Merdeka 312, , Pangandaran, None of the above, Indonesia

High Risk

FDA Import Risk Assessment

51.8
LowModerateHighCritical

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

Statistics

4
Total Refusals
1
Unique Violations
3/28/2005
Latest Refusal
3/28/2005
Earliest Refusal

Score Breakdown

Violation Severity
100.0×40%
Refusal Volume
25.9×30%
Recency
0.0×20%
Frequency
40.0×10%
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

94×

SALMONELLA

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to contain Salmonella, a poisonous and deleterious substance which may render it injurious to health.

Refusal History

DateProductViolationsDivision
3/28/2005
16JGT05SHRIMP & PRAWNS
9SALMONELLA
New England District Office (NWE-DO)
3/28/2005
16JGT05SHRIMP & PRAWNS
9SALMONELLA
New England District Office (NWE-DO)
3/28/2005
16JGT05SHRIMP & PRAWNS
9SALMONELLA
New England District Office (NWE-DO)
3/28/2005
16JGT05SHRIMP & PRAWNS
9SALMONELLA
New England District Office (NWE-DO)

Frequently Asked Questions

What is PT ASI Pudjiastuti's FDA import refusal history?

PT ASI Pudjiastuti (FEI: 3004677781) has 4 FDA import refusal record(s) in our database, spanning from 3/28/2005 to 3/28/2005.

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. PT ASI Pudjiastuti's FEI number is 3004677781.

What types of violations has PT ASI Pudjiastuti received?

PT ASI Pudjiastuti has been cited for 1 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 PT ASI Pudjiastuti come from?

All FDA import refusal data for PT ASI Pudjiastuti 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.