Empresas Carozzi S.A.
FDA import alert and refusal historySantiago, San Bernardo, ChileFEI 3013310671
As of October 26, 2026, Empresas Carozzi S.A. is not on any FDA import alert in SupplierRadar's records; FDA refused 18 of its shipment lines between August 8, 2017 and December 3, 2019, most often for net quantity statement missing (LACKS N/C).
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- Not listed
- Last import refusal
- Spaghetti · NUTRIT LBL
- Last warning letter
- None found
- Last inspection
- Classified NAI (No Action Indicated)
Every FDA record for Empresas Carozzi S.A.
19 records, newest first. Each line links to the FDA page it came from.
2019
- Import refusalRefused, SpaghettiNUTRIT LBLEntry 906-0217456-0Source
- Import refusalSource
Refused, 3 lines in one entry: Granola bars; Gelatin, flavored and 1 moreNUTRIT LBLLACKS N/CEntry CDX-0074955-8Show 3 linesHide lines
- Refused, Granola barsNUTRIT LBLEntry CDX-0074955-8Source
- Refused, Gelatin, flavoredLACKS N/CNUTRIT LBLEntry CDX-0074955-8Source
- Refused, Apricot (pit fruit purees)LACKS N/CNUTRIT LBLEntry CDX-0074955-8Source
2018
- Import refusalRefused, Mixed cereal flakes,shredded and other forms ready to eatNUTRIT LBLEntry CDX-0071183-0Source
2017
- InspectionInspection classified NAI (No Action Indicated)Foodborne Biological HazardsSource
- Import refusalSource
Refused, 13 lines in one entry: Tomato sauce (with other ingredients); Spaghetti and 3 moreLACKS N/CEntry CDX-0069345-9Show 13 linesHide lines
- Refused, Tomato sauce (with other ingredients)LACKS N/CEntry CDX-0069345-9Source
- Refused, Tomato sauce (with other ingredients)LACKS N/CEntry CDX-0069345-9Source
- Refused, SpaghettiLACKS N/CEntry CDX-0069345-9Source
- Refused, Custard pudding (pie) mix, n.e.c.LACKS N/CEntry CDX-0069345-9Source
- Refused, Alimentary pasteLACKS N/CEntry CDX-0069345-9Source
- Refused, Custard pudding (pie) mix, n.e.c.LACKS N/CEntry CDX-0069345-9Source
- Refused, Tomato sauce (with other ingredients)LACKS N/CEntry CDX-0069345-9Source
- Refused, Beverage base, subtropical or tropical fruit, liquidLACKS N/CEntry CDX-0069345-9Source
- Refused, Beverage base, subtropical or tropical fruit, liquidLACKS N/CEntry CDX-0069345-9Source
- Refused, Tomato sauce (with other ingredients)LACKS N/CEntry CDX-0069345-9Source
- Refused, Beverage base, subtropical or tropical fruit, liquidLACKS N/CEntry CDX-0069345-9Source
- Refused, Alimentary pasteLACKS N/CEntry CDX-0069345-9Source
- Refused, Alimentary pasteLACKS N/CEntry CDX-0069345-9Source
Refusal charges, in plain English
- LACKS N/C15 refused lines
Net quantity statement missing
The packaged food appeared not to carry an accurate statement of the quantity of contents, such as net weight, measure, or count, on its label.
- NUTRIT LBL5 refused lines
Nutrition information missing from label
The label or labeling appeared not to carry the nutrition information that U.S. law requires for the food.
Questions about Empresas Carozzi S.A.
- Is Empresas Carozzi S.A. on an FDA import alert?
- No listing for Empresas Carozzi S.A. appears in the FDA import alerts SupplierRadar checked on October 26, 2026. Country-wide alerts may still apply to its products; see the Chile page.
- Has FDA refused shipments from Empresas Carozzi S.A.?
- Yes. FDA refused 18 shipment lines from Empresas Carozzi S.A. between August 8, 2017 and December 3, 2019. The most recent, on December 3, 2019, was spaghetti, charged as NUTRIT LBL (nutrition information missing from label).
- Why did FDA refuse Empresas Carozzi S.A.'s shipments?
- The most frequent charges are LACKS N/C (net quantity statement missing, 15 lines) and NUTRIT LBL (nutrition information missing from label, 5 lines).
- When was Empresas Carozzi S.A. last inspected by FDA?
- FDA's most recent inspection of Empresas Carozzi S.A. with a final classification is dated September 7, 2017 and was classified NAI (No Action Indicated).
- What is Empresas Carozzi S.A.'s FEI number?
- Empresas Carozzi S.A.'s FDA Establishment Identifier (FEI) is 3013310671.
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SupplierRadar is not affiliated with the U.S. Food and Drug Administration. Data comes from public FDA records and may contain errors. This is not legal advice; importers remain responsible for their supplier evaluations.