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S. Achodo

⚠️ Moderate Risk

FEI: 3003629900 • Mutare • ZIMBABWE

FEI

FEI Number

3003629900

📍

Location

Mutare

🇿🇼

Country

ZIMBABWE
🏢

Address

11 Aerodrome Rd, , Mutare, , Zimbabwe

Moderate Risk

FDA Import Risk Assessment

37.7
LowModerateHighCritical

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

Statistics

3
Total Refusals
2
Unique Violations
5/1/2002
Latest Refusal
5/1/2002
Earliest Refusal

Score Breakdown

Violation Severity
70.0×40%
Refusal Volume
22.3×30%
Recency
0.0×20%
Frequency
30.0×10%
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

1792×

AGR RX

The article appears to be a prescription drug manufactured in the U.S. and offered for import by other than the manufacturer and reimportation does not appear to have been authorized by the Secretary for use in a medical emergency.

751×

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).

Refusal History

DateProductViolationsDivision
5/1/2002
66VCP99MISCELLANEOUS PATENT MEDICINES, ETC.
179AGR RX
New Orleans District Office (NOL-DO)
5/1/2002
66VCP99MISCELLANEOUS PATENT MEDICINES, ETC.
179AGR RX
New Orleans District Office (NOL-DO)
5/1/2002
79LRRKIT, FIRST AID
75UNAPPROVED
New Orleans District Office (NOL-DO)

Frequently Asked Questions

What is S. Achodo's FDA import refusal history?

S. Achodo (FEI: 3003629900) has 3 FDA import refusal record(s) in our database, spanning from 5/1/2002 to 5/1/2002.

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. S. Achodo's FEI number is 3003629900.

What types of violations has S. Achodo received?

S. Achodo has been cited for 2 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 S. Achodo come from?

All FDA import refusal data for S. Achodo 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.