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PARAFARMA MEDICAMENTOS E HOSPITA

⚠️ Moderate Risk

FEI: 3039377593 • Redebcao • BRAZIL

FEI

FEI Number

3039377593

📍

Location

Redebcao

🇧🇷

Country

BRAZIL
🏢

Address

Avenida Araguaia, 2106, , Redebcao, , Brazil

Moderate Risk

FDA Import Risk Assessment

41.3
LowModerateHighCritical

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

Statistics

1
Total Refusals
6
Unique Violations
10/9/2025
Latest Refusal
10/9/2025
Earliest Refusal

Score Breakdown

Violation Severity
45.0×40%
Refusal Volume
11.2×30%
Recency
94.9×20%
Frequency
10.0×10%
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

1181×

NOT LISTED

It appears the drug or device is not included in a list required by Section 510(j), or a notice or other information respecting it was not provided as required by section 510(j) or 510(k).

32601×

NO ENGLISH

Required label or labeling appears to not be in English in violation of 21 C.F.R. 801.15(c)(1)

32801×

FRNMFGREG

The article is subject to refusal of admission pursuant to section 801(a)(3) in that it appears to be misbranded as defined in section 502(o) of the FD&C Act. It appears that it was manufactured, prepared, propagated, compounded, or processed in an establishment not duly registered under section 510 of the Act.

3361×

INCONSPICU

Information required by the Act to be on the label or labeling does not appear to be conspicuous enough as to render it likely to be read and understood by the ordinary individual under customary conditions of purchase and use.

3411×

REGISTERED

It appears the device is subject to listing under 510(j) and the initial distributor has not registered as required by 21 CFR 807.20 (a)(5).

5081×

NO 510(K)

The article is subject to refusal of admission pursuant to Section 801(a)(3) in that it is a post 1976 device for which a Section 510(k)application does not appear to have been determined substantially equivalent or otherwise filed.

Refusal History

DateProductViolationsDivision
10/9/2025
80FMFSYRINGE, PISTON
118NOT LISTED
3260NO ENGLISH
3280FRNMFGREG
336INCONSPICU
341REGISTERED
508NO 510(K)
Division of Southeast Imports (DSEI)

Frequently Asked Questions

What is PARAFARMA MEDICAMENTOS E HOSPITA's FDA import refusal history?

PARAFARMA MEDICAMENTOS E HOSPITA (FEI: 3039377593) has 1 FDA import refusal record(s) in our database, spanning from 10/9/2025 to 10/9/2025.

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. PARAFARMA MEDICAMENTOS E HOSPITA's FEI number is 3039377593.

What types of violations has PARAFARMA MEDICAMENTOS E HOSPITA received?

PARAFARMA MEDICAMENTOS E HOSPITA 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 PARAFARMA MEDICAMENTOS E HOSPITA come from?

All FDA import refusal data for PARAFARMA MEDICAMENTOS E HOSPITA 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.