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Robinson Pharma, Inc.

⚠️ Moderate Risk

FEI: 3008408934 • Santa Ana, CA • UNITED STATES

FEI

FEI Number

3008408934

📍

Location

Santa Ana, CA

🇺🇸
🏢

Address

3330 S Harbor Blvd, , Santa Ana, CA, United States

Moderate Risk

FDA Import Risk Assessment

34.8
LowModerateHighCritical

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

Statistics

10
Total Refusals
8
Unique Violations
6/26/2017
Latest Refusal
10/5/2001
Earliest Refusal

Score Breakdown

Violation Severity
56.4×40%
Refusal Volume
38.6×30%
Recency
0.0×20%
Frequency
6.4×10%
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

753×

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).

4883×

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.

2182×

LIST INGRE

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)(2) of the FD&C Act in that it is fabricated from two or more ingredients and the label fails to bear the common or usual name of each such ingredient and/or the article purports to be a beverage containing vegetable or fruit juice, but does not bear a statement with appropriate prominence on the information panel of the total percentage of such fruit or vegetable juice contained in the food.

3202×

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.

4731×

LABELING

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

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.

3241×

NO ENGLISH

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)).

3081×

MFR INSAN

The article is subject to refusal of admission pursuant to section 801(a)(1) in that the article appears to have been manufactured, processed, or packed under insanitary conditions.

Refusal History

DateProductViolationsDivision
6/26/2017
41YHH99DIETARY CONVENTIONAL FOODS, N.E.C.
308MFR INSAN
Division of West Coast Imports (DWCI)
10/26/2016
64RDH18HUMAN GROWTH HORMONE (HORMONE)
75UNAPPROVED
Cincinnati District Office (CIN-DO)
2/10/2009
54ACA90MULTIPLE VITAMINS (MVI-12 VITAMIN COMBO) (VITAMIN)
218LIST INGRE
324NO ENGLISH
Los Angeles District Office (LOS-DO)
4/22/2008
54ECR99HERBALS & BOTANICAL TEAS, N.E.C.
320LACKS FIRM
Los Angeles District Office (LOS-DO)
4/22/2008
54ECR99HERBALS & BOTANICAL TEAS, N.E.C.
320LACKS FIRM
Los Angeles District Office (LOS-DO)
2/22/2008
54YCZ99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
218LIST INGRE
473LABELING
75UNAPPROVED
Los Angeles District Office (LOS-DO)
3/27/2007
54YCH99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
482NUTRIT LBL
New Orleans District Office (NOL-DO)
3/30/2005
54FBY02ALFALFA (HERBAL & BOTANICALS, NOT TEAS)
488HEALTH C
Los Angeles District Office (LOS-DO)
10/5/2001
54YCA99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
488HEALTH C
75UNAPPROVED
Los Angeles District Office (LOS-DO)
10/5/2001
54YCA99VITAMIN, MINERAL, PROTEINS AND UNCONVENTIONAL DIETARY SPECIALITIES FOR HUMANS AND ANIMALS, N.E.C.
488HEALTH C
Los Angeles District Office (LOS-DO)

Frequently Asked Questions

What is Robinson Pharma, Inc.'s FDA import refusal history?

Robinson Pharma, Inc. (FEI: 3008408934) has 10 FDA import refusal record(s) in our database, spanning from 10/5/2001 to 6/26/2017.

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. Robinson Pharma, Inc.'s FEI number is 3008408934.

What types of violations has Robinson Pharma, Inc. received?

Robinson Pharma, Inc. has been cited for 8 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 Robinson Pharma, Inc. come from?

All FDA import refusal data for Robinson Pharma, Inc. 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.