P.P.H.U.
⚠️ Moderate Risk
FEI: 3004293222 • Fabianki, Kujawsko-Pomorskie • POLAND
FEI Number
3004293222
Location
Fabianki, Kujawsko-Pomorskie
Country
POLANDAddress
Ul. Nasiegniewo 40, , Fabianki, Kujawsko-Pomorskie, Poland
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
Statistics
Score Breakdown
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
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.
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).
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.
UNSAFE ADD
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to bear or contain an unsafe food additive within the meaning of section 409.
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.
USUAL NAME
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)(1) of the FD&C Act in that the label fails to bear the common or usual name of the food, if any there be.
FILTHY
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the article appears to consist in whole or in part of a filthy, putrid, or decomposed substance or be otherwise unfit for food.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 11/16/2005 | 07BGT02CORN CHIPS, FRIED | Detroit District Office (DET-DO) | |
| 11/16/2005 | 24FCP20CUCUMBERS (FRUIT USED AS VEGETABLE) | 249FILTHY | Detroit District Office (DET-DO) |
| 1/8/2005 | 24VCP11CELERY, WITH SAUCE | 83NO PROCESS | Chicago District Office (CHI-DO) |
| 1/8/2005 | 24VCP11CELERY, WITH SAUCE | 83NO PROCESS | Chicago District Office (CHI-DO) |
| 1/8/2005 | 24FCP20CUCUMBERS (FRUIT USED AS VEGETABLE) | Chicago District Office (CHI-DO) | |
| 1/8/2005 | 25PCP99MUSHROOMS AND OTHER FUNGI PRODUCTS, WHOLE (BUTTON), N.E.C. | Chicago District Office (CHI-DO) | |
| 1/8/2005 | 25PCP99MUSHROOMS AND OTHER FUNGI PRODUCTS, WHOLE (BUTTON), N.E.C. | Chicago District Office (CHI-DO) | |
| 1/8/2005 | 24VCP99LEAF & STEM VEGETABLES, WITH SAUCE, N.E.C. | Chicago District Office (CHI-DO) | |
| 1/8/2005 | 24VCP04BEET TOPS, WITH SAUCE | Chicago District Office (CHI-DO) | |
| 1/8/2005 | 24KCI07PEPPER, SWEET, WITH SAUCE | Chicago District Office (CHI-DO) | |
| 1/12/2004 | 24FCP04PIMIENTO PEPPER (FRUIT USED AS VEGETABLE) | Detroit District Office (DET-DO) |
Frequently Asked Questions
What is P.P.H.U.'s FDA import refusal history?
P.P.H.U. (FEI: 3004293222) has 11 FDA import refusal record(s) in our database, spanning from 1/12/2004 to 11/16/2005.
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. P.P.H.U.'s FEI number is 3004293222.
What types of violations has P.P.H.U. received?
P.P.H.U. 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 P.P.H.U. come from?
All FDA import refusal data for P.P.H.U. 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.