PARTEL (INDIA) CORPORATION
⚠️ Moderate Risk
FEI: 3002535455 • Mumbai, Maharashtra • INDIA
FEI Number
3002535455
Location
Mumbai, Maharashtra
Country
INDIAAddress
Sharda Chambers, 31 V Thackersey Marg; Po Box No 5079, Mumbai, Maharashtra, India
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
FILTHY
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the article appears to consist in whole or in part of a filthy, putrid, or decomposed substance or be otherwise unfit for food.
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).
UNSAFE COL
The article appears to be, or to bear or contain a color additive which is unsafe within the meaning of Section 721(a).
NEEDS FCE
It appears the manufacturer is not registered as a low acid canned food or acidified food manufacturer pursuant to 21 CFR 108.25(c)(1) or 108.35(c)(1).
NO PROCESS
The article is subject to refusal of admission pursuant to Section 801(a)(3) in that the manufacturer's failure to file a scheduled process demonstrates that the product is not being manufactured under the mandatory provisions of 21 CFR Part 108 and therefore appears to have been manufactured, processed, or packed, under insanitary conditions whereby it may have been rendered injurious to health.
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.
DIRECTIONS
The article is subject to refusal of admission pursuant to section 801(a)(3) in that it is a device whose label appears to not bear adequate directions for use.
Refusal History
| Date | Product | Violations | Division |
|---|---|---|---|
| 4/15/2008 | 03AHT03BISCUITS | 249FILTHY | Southwest Import District Office (SWI-DO) |
| 3/8/2007 | 21HHH05DATES, DRIED OR PASTE | Chicago District Office (CHI-DO) | |
| 1/25/2007 | 12CEY99CHEESE PRODUCTS, NON-STANDARDIZED, N.E.C. | Los Angeles District Office (LOS-DO) | |
| 1/19/2006 | 28AGT37POPPYSEED, WHOLE (SPICE) | 249FILTHY | Chicago District Office (CHI-DO) |
| 1/19/2006 | 28YGT99SPICES, FLAVORS AND SALT NOT MENTIONED ELSEWHERE, N.E.C. | 249FILTHY | Chicago District Office (CHI-DO) |
| 11/16/2005 | 63RBY04SODIUM FLUORIDE (DENTAL CARIES PROPHYLACTIC) | 118NOT LISTED | Los Angeles District Office (LOS-DO) |
| 6/2/2005 | 33EGT06FLAVORED CANDY, HARD (LIVE SAVERS, ETC.), WITHOUT NUTS AND FRUIT (WITHOUT CHOCOLATE) | 249FILTHY | Southwest Import District Office (SWI-DO) |
| 7/16/2002 | 03HHT08BUTTER/BUTTER FLAVORED,PLAIN COOKIES,BISCUITS AND WAFERS | 249FILTHY | Southwest Import District Office (SWI-DO) |
| 1/3/2002 | 60LBJ99ANALGESIC, N.E.C. | New York District Office (NYK-DO) |
Frequently Asked Questions
What is PARTEL (INDIA) CORPORATION's FDA import refusal history?
PARTEL (INDIA) CORPORATION (FEI: 3002535455) has 9 FDA import refusal record(s) in our database, spanning from 1/3/2002 to 4/15/2008.
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. PARTEL (INDIA) CORPORATION's FEI number is 3002535455.
What types of violations has PARTEL (INDIA) CORPORATION received?
PARTEL (INDIA) CORPORATION 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 PARTEL (INDIA) CORPORATION come from?
All FDA import refusal data for PARTEL (INDIA) CORPORATION 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.