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THE LITTLEOAK COMPANY PTY CO

⚠️ High Risk

FEI: 3027036124 • Byron Bay, New South Wales • AUSTRALIA

FEI

FEI Number

3027036124

📍

Location

Byron Bay, New South Wales

🇦🇺

Country

AUSTRALIA
🏢

Address

U 1 120 Jonson St, , Byron Bay, New South Wales, Australia

High Risk

FDA Import Risk Assessment

54.5
LowModerateHighCritical

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

Statistics

21
Total Refusals
6
Unique Violations
9/19/2023
Latest Refusal
6/21/2023
Earliest Refusal

Score Breakdown

Violation Severity
47.0×40%
Refusal Volume
49.7×30%
Recency
53.8×20%
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

32112×

LACKS N/C

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)(2) of the FD&C Act in that the food is in package form and the label fails to bear an accurate statement of the quantity of the contents in terms of weight, measure, or numerical count in accordance with Section 403(e)(2) of the FD&C Act.

48211×

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.

21608×

LACK NOTIF

Adulterated, 801(a)(3), lack of documentation establishing that the infant formula meets all notification conditions required by 412(c) or 412(d), Prohibited Act, Section 301(s).

4737×

LABELING

The article appears in violation of FPLA because of its placement, form and/or contents statement.

2605×

FALSE

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(a)(1 ) of the FD&C Act in that the labeling is false or misleading in any particular.

33611×

NUTR DEF

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the infant formula appears to adulterated in that it does not provide the nutrients required by 21 CFR 107.100

Refusal History

DateProductViolationsDivision
9/19/2023
40PYY99OTHER FORMULA PRODUCTS, N.E.C., POWDER FORMULA
2160LACK NOTIF
321LACKS N/C
482NUTRIT LBL
Division of Southeast Imports (DSEI)
7/31/2023
40PYY99OTHER FORMULA PRODUCTS, N.E.C., POWDER FORMULA
3361NUTR DEF
Division of Southeast Imports (DSEI)
7/31/2023
40PYT99OTHER FORMULA PRODUCTS, N.E.C., POWDER FORMULA
2160LACK NOTIF
321LACKS N/C
482NUTRIT LBL
Division of Southeast Imports (DSEI)
7/27/2023
40PYY99OTHER FORMULA PRODUCTS, N.E.C., POWDER FORMULA
473LABELING
Division of Southeast Imports (DSEI)
7/27/2023
40PYT99OTHER FORMULA PRODUCTS, N.E.C., POWDER FORMULA
473LABELING
Division of Southeast Imports (DSEI)
7/27/2023
40PYT99OTHER FORMULA PRODUCTS, N.E.C., POWDER FORMULA
473LABELING
Division of Southeast Imports (DSEI)
7/27/2023
40PYT99OTHER FORMULA PRODUCTS, N.E.C., POWDER FORMULA
473LABELING
Division of Southeast Imports (DSEI)
7/27/2023
40PYT99OTHER FORMULA PRODUCTS, N.E.C., POWDER FORMULA
473LABELING
Division of Southeast Imports (DSEI)
7/27/2023
40PYT99OTHER FORMULA PRODUCTS, N.E.C., POWDER FORMULA
473LABELING
Division of Southeast Imports (DSEI)
7/27/2023
40PYT99OTHER FORMULA PRODUCTS, N.E.C., POWDER FORMULA
473LABELING
Division of Southeast Imports (DSEI)
7/20/2023
40PYT99OTHER FORMULA PRODUCTS, N.E.C., POWDER FORMULA
2160LACK NOTIF
Division of Southeast Imports (DSEI)
7/16/2023
40PYT99OTHER FORMULA PRODUCTS, N.E.C., POWDER FORMULA
260FALSE
321LACKS N/C
482NUTRIT LBL
Division of Southeast Imports (DSEI)
7/16/2023
40PYY01MILK BASE INFANT FORMULA PRODUCT (0-12 MONTHS), POWDER FORMULA
260FALSE
321LACKS N/C
482NUTRIT LBL
Division of Southeast Imports (DSEI)
7/16/2023
40PYT01MILK BASE INFANT FORMULA PRODUCT (0-12 MONTHS), POWDER FORMULA
260FALSE
321LACKS N/C
482NUTRIT LBL
Division of Southeast Imports (DSEI)
7/16/2023
40PYY01MILK BASE INFANT FORMULA PRODUCT (0-12 MONTHS), POWDER FORMULA
260FALSE
321LACKS N/C
482NUTRIT LBL
Division of Southeast Imports (DSEI)
7/14/2023
40PYT99OTHER FORMULA PRODUCTS, N.E.C., POWDER FORMULA
260FALSE
321LACKS N/C
Division of Southeast Imports (DSEI)
7/13/2023
40PYT99OTHER FORMULA PRODUCTS, N.E.C., POWDER FORMULA
2160LACK NOTIF
321LACKS N/C
482NUTRIT LBL
Division of Southeast Imports (DSEI)
7/13/2023
40PYT99OTHER FORMULA PRODUCTS, N.E.C., POWDER FORMULA
2160LACK NOTIF
321LACKS N/C
482NUTRIT LBL
Division of Southeast Imports (DSEI)
7/5/2023
40PYY01MILK BASE INFANT FORMULA PRODUCT (0-12 MONTHS), POWDER FORMULA
2160LACK NOTIF
321LACKS N/C
482NUTRIT LBL
Division of Southeast Imports (DSEI)
6/21/2023
40PYT99OTHER FORMULA PRODUCTS, N.E.C., POWDER FORMULA
2160LACK NOTIF
321LACKS N/C
482NUTRIT LBL
Division of Southeast Imports (DSEI)
6/21/2023
40PYY99OTHER FORMULA PRODUCTS, N.E.C., POWDER FORMULA
2160LACK NOTIF
321LACKS N/C
482NUTRIT LBL
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is THE LITTLEOAK COMPANY PTY CO's FDA import refusal history?

THE LITTLEOAK COMPANY PTY CO (FEI: 3027036124) has 21 FDA import refusal record(s) in our database, spanning from 6/21/2023 to 9/19/2023.

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. THE LITTLEOAK COMPANY PTY CO's FEI number is 3027036124.

What types of violations has THE LITTLEOAK COMPANY PTY CO received?

THE LITTLEOAK COMPANY PTY CO has been cited for 6 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 THE LITTLEOAK COMPANY PTY CO come from?

All FDA import refusal data for THE LITTLEOAK COMPANY PTY CO 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.