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Peck Srl

⚠️ Moderate Risk

FEI: 1000176441 • Milan, Milan • ITALY

FEI

FEI Number

1000176441

📍

Location

Milan, Milan

🇮🇹

Country

ITALY
🏢

Address

Via Spadari 9, , Milan, Milan, Italy

Moderate Risk

FDA Import Risk Assessment

38.7
LowModerateHighCritical

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

Statistics

7
Total Refusals
4
Unique Violations
8/5/2003
Latest Refusal
1/9/2002
Earliest Refusal

Score Breakdown

Violation Severity
60.6×40%
Refusal Volume
33.5×30%
Recency
0.0×20%
Frequency
44.6×10%
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

836×

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.

4824×

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.

2563×

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)).

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).

Refusal History

DateProductViolationsDivision
8/5/2003
21GCT09OLIVES (PIT FRUIT)
83NO PROCESS
Baltimore District Office (BLT-DO)
8/5/2003
21GCT09OLIVES (PIT FRUIT)
83NO PROCESS
Baltimore District Office (BLT-DO)
7/16/2003
25PCH99MUSHROOMS AND OTHER FUNGI PRODUCTS, WHOLE (BUTTON), N.E.C.
83NO PROCESS
Baltimore District Office (BLT-DO)
1/7/2003
25ECE99MIXED VEGETABLES, N.E.C.
256INCONSPICU
482NUTRIT LBL
62NEEDS FCE
83NO PROCESS
Southwest Import District Office (SWI-DO)
12/19/2002
25JCE25ONION BULB (YELLOW, WHITE, RED, ETC.) (ROOT & TUBER VEGETABLE)
256INCONSPICU
482NUTRIT LBL
62NEEDS FCE
83NO PROCESS
Southwest Import District Office (SWI-DO)
12/19/2002
25ECE99MIXED VEGETABLES, N.E.C.
256INCONSPICU
482NUTRIT LBL
62NEEDS FCE
83NO PROCESS
Southwest Import District Office (SWI-DO)
1/9/2002
03RFT01CAKE WITHOUT CUSTARD OR CREAM FILLING
482NUTRIT LBL
Southwest Import District Office (SWI-DO)

Frequently Asked Questions

What is Peck Srl's FDA import refusal history?

Peck Srl (FEI: 1000176441) has 7 FDA import refusal record(s) in our database, spanning from 1/9/2002 to 8/5/2003.

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. Peck Srl's FEI number is 1000176441.

What types of violations has Peck Srl received?

Peck Srl 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 Peck Srl come from?

All FDA import refusal data for Peck Srl 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.