Manakamana Exports
⚠️ Moderate Risk
FEI: 3005318005 • Kathmandu, Kathmandu • NEPAL
FEI Number
3005318005
Location
Kathmandu, Kathmandu
Country
NEPALAddress
Thamel, , Kathmandu, Kathmandu, Nepal
Moderate Risk
FDA Import Risk Assessment
This firm has a moderate history of FDA import refusals. Some attention may be warranted.
Statistics
Score Breakdown
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
USUAL NAME
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)(1) of the FD&C Act in that the label fails to bear the common or usual name of the food, if any there be.
CSTIC LBLG
The labeling appears to fail to comply with cosmetic labeling requirements of Section 602(a), and/or (b), and/or (c), and as identified by 21 C.F.R. Part 701.
LACKS N/C
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)(2) of the FD&C Act in that the food is in package form and the label fails to bear an accurate statement of the quantity of the contents in terms of weight, measure, or numerical count in accordance with Section 403(e)(2) of the FD&C Act.
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.
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.
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.
LABELING
The article appears in violation of FPLA because of its placement, form and/or contents statement.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 7/31/2009 | 53LH99OTHER SKIN CARE PREPARATIONS, N.E.C. | 471CSTIC LBLG | Southwest Import District Office (SWI-DO) |
| 7/31/2009 | 53ED01HAIR CONDITIONERS (HAIR PREPARATIONS, NON-COLORING) | 471CSTIC LBLG | Southwest Import District Office (SWI-DO) |
| 7/31/2009 | 53LH99OTHER SKIN CARE PREPARATIONS, N.E.C. | 471CSTIC LBLG | Southwest Import District Office (SWI-DO) |
| 7/31/2009 | 28SGT03SALT, ROCK (TABLE SALT) | Southwest Import District Office (SWI-DO) | |
| 7/31/2009 | 02AGT99GRAIN, WHOLE, N.E.C. | Southwest Import District Office (SWI-DO) | |
| 7/31/2009 | 33EGT99HARD CANDY WITHOUT NUTS AND FRUIT, N.E.C. (WITHOUT CHOCOLATE) | Southwest Import District Office (SWI-DO) |
Frequently Asked Questions
What is Manakamana Exports's FDA import refusal history?
Manakamana Exports (FEI: 3005318005) has 6 FDA import refusal record(s) in our database, spanning from 7/31/2009 to 7/31/2009.
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. Manakamana Exports's FEI number is 3005318005.
What types of violations has Manakamana Exports received?
Manakamana Exports has been cited for 7 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 Manakamana Exports come from?
All FDA import refusal data for Manakamana Exports 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.