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Permex Producer & Exporter Corp.

⚠️ Moderate Risk

FEI: 1000158350 • Malate • PHILIPPINES

FEI

FEI Number

1000158350

📍

Location

Malate

🇵🇭
🏢

Address

J. Napkil St., Suite 4F Vermont Towers, Malate, , Philippines

Moderate Risk

FDA Import Risk Assessment

25.6
LowModerateHighCritical

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

Statistics

3
Total Refusals
4
Unique Violations
12/3/2009
Latest Refusal
3/29/2004
Earliest Refusal

Score Breakdown

Violation Severity
46.0×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
5.3×10%
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

4822×

NUTRIT LBL

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be misbranded in that the label or labeling fails to bear the required nutrition information.

2181×

LIST INGRE

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(i)(2) of the FD&C Act in that it is fabricated from two or more ingredients and the label fails to bear the common or usual name of each such ingredient and/or the article purports to be a beverage containing vegetable or fruit juice, but does not bear a statement with appropriate prominence on the information panel of the total percentage of such fruit or vegetable juice contained in the food.

2561×

INCONSPICU

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(f) of the FD&C Act in that any word, statement, or other information required by or under the authority of the FD&C Act to appear on the label or labeling is not prominently placed thereon with such conspicuousness (as compared with other words, statements, designs, or devices, in the labeling) and in such terms as to render it likely to be read and understood by the ordinary individual under customary terms of purchase and use (for example, label contains information in two or more languages but fails to repeat all required information in both languages in accordance with 21 CFR 101.15(c)(2), or label fails to include all required information in English in accordance with 21 CFR 101.15(c)(1), except in the case of articles distributed solely in the Commonwealth of Puerto Rico or in a Territory where the predominant language is one other than English)).

831×

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.

Refusal History

DateProductViolationsDivision
12/3/2009
16AET45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.)
218LIST INGRE
482NUTRIT LBL
New York District Office (NYK-DO)
9/15/2008
16MEE03SQUID, OTHER AQUATIC SPECIES
83NO PROCESS
San Francisco District Office (SAN-DO)
3/29/2004
16AEE45TUNA (ALBACORE, YELLOWFIN, BLUEFIN, SKIPJACK, ETC.)
256INCONSPICU
482NUTRIT LBL
New York District Office (NYK-DO)

Frequently Asked Questions

What is Permex Producer & Exporter Corp.'s FDA import refusal history?

Permex Producer & Exporter Corp. (FEI: 1000158350) has 3 FDA import refusal record(s) in our database, spanning from 3/29/2004 to 12/3/2009.

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. Permex Producer & Exporter Corp.'s FEI number is 1000158350.

What types of violations has Permex Producer & Exporter Corp. received?

Permex Producer & Exporter Corp. has been cited for 4 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 Permex Producer & Exporter Corp. come from?

All FDA import refusal data for Permex Producer & Exporter Corp. 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.