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Celeste(S) Private Limited

⚠️ Moderate Risk

FEI: 3005829728 • Singaore • SINGAPORE

FEI

FEI Number

3005829728

📍

Location

Singaore

🇸🇬

Country

SINGAPORE
🏢

Address

56 Minbu Road #06-03 Mindu Villa, , Singaore, , Singapore

Moderate Risk

FDA Import Risk Assessment

29.3
LowModerateHighCritical

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

Statistics

2
Total Refusals
4
Unique Violations
8/9/2006
Latest Refusal
8/9/2006
Earliest Refusal

Score Breakdown

Violation Severity
55.0×40%
Refusal Volume
17.7×30%
Recency
0.0×20%
Frequency
20.0×10%
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

2371×

NO PMA

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the device appears to be a Class III device and does not appear to have in effect an approved application for premarket approval pursuant to Section 515 of the Act, or an exemption pursuant to Section 520(g)(1).

3201×

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.

4821×

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.

841×

RX DEVICE

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it is a prescription device that appears to not feature a prescription device legend as required by 21 CFR 801.109.

Refusal History

DateProductViolationsDivision
8/9/2006
54ABA99VITAMIN, N.E.C.
320LACKS FIRM
482NUTRIT LBL
New Orleans District Office (NOL-DO)
8/9/2006
89KTBDEVICE, IONTOPHORESIS, SPECIFIC USES
237NO PMA
84RX DEVICE
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is Celeste(S) Private Limited's FDA import refusal history?

Celeste(S) Private Limited (FEI: 3005829728) has 2 FDA import refusal record(s) in our database, spanning from 8/9/2006 to 8/9/2006.

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. Celeste(S) Private Limited's FEI number is 3005829728.

What types of violations has Celeste(S) Private Limited received?

Celeste(S) Private Limited 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 Celeste(S) Private Limited come from?

All FDA import refusal data for Celeste(S) Private Limited 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.