Grupo Cimer S.P.R. DE R.I.
FDA import alert and refusal historyJiutepec, MexicoFEI 3007218518
As of October 27, 2026, Grupo Cimer S.P.R. DE R.I. (Jiutepec, Mexico) is on the red list of FDA Import Alert 99-35 (Fresh produce: insanitary conditions) for basil, published by FDA on June 24, 2021, and has 6 FDA import refusals recorded since October 2016.
Data from FDA public records, last checked . Request a correction
Current status
- Import alerts
- IA 99-35 · red list
- Last import refusal
- Basil (sweet basil), whole (spice) · MFR INSAN
- Last warning letter
- None found
- Last inspection
- None on record
Every FDA record for Grupo Cimer S.P.R. DE R.I.
7 records, newest first. Each line links to the FDA page it came from.
2022
2021
- Import refusalSource
Refused, 3 lines in one entry: Basil (sweet basil), whole (spice)MFR INSANMFR INJEntry UT4-0206496-8Show 3 linesHide lines
- Import alert listingListed on Import Alert 99-35red listBasilSource
Refusal charges, in plain English
- MFR INJ6 refused lines
Insanitary conditions, may be injurious
The product appeared to have been prepared, packed, or held under insanitary conditions whereby it may have been rendered injurious to health.
- MFR INSAN6 refused lines
Insanitary manufacturing, processing or packing
The product appeared to have been manufactured, processed, or packed under insanitary conditions, which is a ground for refusal under section 801(a)(1) of the FD&C Act.
Questions about Grupo Cimer S.P.R. DE R.I.
- Is Grupo Cimer S.P.R. DE R.I. on an FDA import alert?
- Yes. As of October 27, 2026, Grupo Cimer S.P.R. DE R.I. is on the red list of FDA Import Alert 99-35, “Fresh produce: insanitary conditions”, for basil; FDA published the listing on June 24, 2021.
- Has FDA refused shipments from Grupo Cimer S.P.R. DE R.I.?
- Yes. FDA refused 6 shipment lines from Grupo Cimer S.P.R. DE R.I. between July 12, 2021 and January 20, 2022. The most recent, on January 20, 2022, was basil (sweet basil), whole (spice), charged as MFR INSAN (insanitary manufacturing, processing or packing).
- Why did FDA refuse Grupo Cimer S.P.R. DE R.I.'s shipments?
- The most frequent charges are MFR INJ (insanitary conditions, may be injurious, 6 lines) and MFR INSAN (insanitary manufacturing, processing or packing, 6 lines).
- What is Grupo Cimer S.P.R. DE R.I.'s FEI number?
- Grupo Cimer S.P.R. DE R.I.'s FDA Establishment Identifier (FEI) is 3007218518.
- Can shipments from Grupo Cimer S.P.R. DE R.I. still enter the U.S.?
- Shipments of basil from Grupo Cimer S.P.R. DE R.I. can be detained without physical examination under Import Alert 99-35; FDA releases them only if evidence shows they do not have the listed violation. Importers must consider this listing in their FSVP evaluation (21 CFR 1.505).
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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.