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M/s Herbsforever

⚠️ Moderate Risk

FEI: 3010964548 • Amritsar, Punjab • INDIA

FEI

FEI Number

3010964548

📍

Location

Amritsar, Punjab

🇮🇳

Country

INDIA
🏢

Address

Plot no. 9 f, Bal Kalan, Majitha Road, , Amritsar, Punjab, India

Moderate Risk

FDA Import Risk Assessment

45.8
LowModerateHighCritical

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

Statistics

9
Total Refusals
6
Unique Violations
5/8/2015
Latest Refusal
5/8/2015
Earliest Refusal

Score Breakdown

Violation Severity
64.2×40%
Refusal Volume
37.0×30%
Recency
0.0×20%
Frequency
90.0×10%
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

754×

UNAPPROVED

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it appears to be a new drug within the meaning of Section 201(p) without an approved New Drug Application (NDA).

38622×

DIETARYING

The article is subject to refusal of admission pursuant to Section 801(a)(3) of the FD&C Act in that it is a dietary supplement that appears to be misbranded within the meaning of Section 403(s)(2)(A) of the FD&C Act in that the dietary supplement label or labeling fails to list the name of each dietary ingredient of the supplement and the quantity of each such dietary ingredient or , with respect to a proprietary blend of such dietary ingredients, the total quantity of all dietary ingredients in the blend.

4732×

LABELING

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

4882×

HEALTH C

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 bears an unauthorized nutrient content/health claim.

2601×

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.

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.

Refusal History

DateProductViolationsDivision
5/8/2015
54FBR99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
3862DIETARYING
473LABELING
San Francisco District Office (SAN-DO)
5/8/2015
54FBE99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
488HEALTH C
San Francisco District Office (SAN-DO)
5/8/2015
54FBE99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
488HEALTH C
San Francisco District Office (SAN-DO)
5/8/2015
54FBR99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
473LABELING
482NUTRIT LBL
San Francisco District Office (SAN-DO)
5/8/2015
54FBE99HERBALS & BOTANICALS (NOT TEAS), N.E.C.
260FALSE
3862DIETARYING
San Francisco District Office (SAN-DO)
5/8/2015
66VBR99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
San Francisco District Office (SAN-DO)
5/8/2015
66VBR99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
San Francisco District Office (SAN-DO)
5/8/2015
66VBR99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
San Francisco District Office (SAN-DO)
5/8/2015
66VBY99MISCELLANEOUS PATENT MEDICINES, ETC.
75UNAPPROVED
San Francisco District Office (SAN-DO)

Frequently Asked Questions

What is M/s Herbsforever's FDA import refusal history?

M/s Herbsforever (FEI: 3010964548) has 9 FDA import refusal record(s) in our database, spanning from 5/8/2015 to 5/8/2015.

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. M/s Herbsforever's FEI number is 3010964548.

What types of violations has M/s Herbsforever received?

M/s Herbsforever 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 M/s Herbsforever come from?

All FDA import refusal data for M/s Herbsforever 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.